chr2:234183368:A>G Detail (hg19) (ATG16L1)

Information

Genome

Assembly Position
hg19 chr2:234,183,368-234,183,368
hg38 chr2:233,274,722-233,274,722 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_198890.2:c.409A>G NP_942593.2:p.Thr137Ala
NM_001190266.1:c.898A>G NP_001177195.1:p.Thr300Ala
NM_001190267.1:c.898A>G NP_001177196.1:p.Thr300Ala
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:0.246
ToMMo:0.220
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:0.333

Prediction

ClinVar

Clinical Significance Benign
Review star
Show details
Links
Type Database ID Link
Gene MIM 610767 OMIM
HGNC 21498 HGNC
Ensembl ENSG00000085978 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv10904373 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
risk factor 2014-02-27 no assertion criteria provided Inflammatory bowel disease 10, susceptibility to germline Detail
Benign 2015-02-24 criteria provided, single submitter not specified germline Detail
Benign 2019-10-17 criteria provided, single submitter ATG16L1-related disorder germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
<0.001 obesity Prior to multiple testing correction, univariate analysis associated APOE rs4293... BeFree 26043189 Detail
0.008 obesity Prior to multiple testing correction, univariate analysis associated APOE rs4293... BeFree 26043189 Detail
0.196 obesity Prior to multiple testing correction, univariate analysis associated APOE rs4293... BeFree 26043189 Detail
0.368 Crohn Disease Detection of Mycobacterium avium subspecies paratuberculosis in patients with Cr... BeFree 24522266 Detail
0.145 Crohn Disease Detection of Mycobacterium avium subspecies paratuberculosis in patients with Cr... BeFree 24522266 Detail
0.368 Crohn Disease To investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and... BeFree 20066736 Detail
0.371 Crohn Disease To investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and... BeFree 20066736 Detail
0.560 Crohn Disease To investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and... BeFree 20066736 Detail
0.050 Crohn Disease To investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and... BeFree 20066736 Detail
0.170 Crohn Disease The aim of this study was to determine the role of the ATG16L1 (rs2241880) and I... BeFree 19491842 Detail
0.368 Crohn Disease The aim of this study was to determine the role of the ATG16L1 (rs2241880) and I... BeFree 19491842 Detail
0.124 ulcerative colitis In conclusion, our results confirm the ATG16L1 rs2241880 and IRGM rs13361189 and... BeFree 19491842 Detail
0.033 ulcerative colitis In conclusion, our results confirm the ATG16L1 rs2241880 and IRGM rs13361189 and... BeFree 19491842 Detail
0.080 Crohn Disease We confirmed a strong association between three NOD2/CARD15 gene variants (Pro26... BeFree 18715515 Detail
0.560 Crohn Disease We confirmed a strong association between three NOD2/CARD15 gene variants (Pro26... BeFree 18715515 Detail
0.080 Crohn Disease We confirmed a strong association between three NOD2/CARD15 gene variants (Pro26... BeFree 18715515 Detail
0.368 Crohn Disease We confirmed a strong association between three NOD2/CARD15 gene variants (Pro26... BeFree 18715515 Detail
0.368 Crohn Disease The ATG16L1 gene variants rs2241879 and rs2241880 (T300A) are strongly associate... BeFree 18162085 Detail
0.033 ulcerative colitis In addition, the carriage of T300A variant alleles conferred a protective effect... BeFree 25159710 Detail
0.368 Crohn Disease However a possible role of ATG16L1 (T300A) on CD phenotype was suggested. BeFree 25159710 Detail
0.368 Crohn Disease A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibi... GWASCAT 22412388 Detail
0.368 Crohn Disease Genome-wide association studies have described an association of the ATG16L1 (au... BeFree 19659808 Detail
0.033 ulcerative colitis The ATG16L1 T300A polymorphism contributes to susceptibility to CD and UC in adu... BeFree 20222171 Detail
0.397 Inflammatory Bowel Diseases Our aims were: to replicate the ATG16L1 Thr300Ala association with inflammatory ... BeFree 19575361 Detail
0.560 Crohn Disease We found a statistically significant interaction with respect to Crohn disease r... BeFree 17200669 Detail
0.368 Crohn Disease Publications addressing the relationship between rs2241880/T300A polymorphism of... BeFree 20222171 Detail
0.368 Crohn Disease Thr300Ala polymorphism in ATG16L1 was reported as a susceptibility factor to Cro... BeFree 19575361 Detail
0.033 ulcerative colitis With respect to ATG16L1, the G allele of SNP rs2241880 has been shown in multipl... BeFree 18366306 Detail
0.340 Inflammatory Bowel Diseases Our aims were: to replicate the ATG16L1 Thr300Ala association with inflammatory ... BeFree 19575361 Detail
0.173 Inflammatory Bowel Diseases T300A polymorphism of ATG16L1 and susceptibility to inflammatory bowel diseases:... BeFree 20222171 Detail
0.120 Crohn Disease A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibi... GWASCAT 22412388 Detail
0.120 Crohn Disease Genome-wide association study identifies new susceptibility loci for Crohn disea... GWASCAT 17435756 Detail
0.368 Crohn Disease ATG16L1 T300A polymorphism and Crohn's disease susceptibility: evidence from 13,... BeFree 19337756 Detail
0.173 Inflammatory Bowel Diseases ATG16L1 T300A shows strong associations with disease subgroups in a large Austra... BeFree 18671817 Detail
<0.001 irritable bowel syndrome ATG16L1 T300A shows strong associations with disease subgroups in a large Austra... BeFree 18671817 Detail
0.173 Inflammatory Bowel Diseases Role of ATG16L1 Thr300Ala polymorphism in inflammatory bowel disease: a Study in... BeFree 19575361 Detail
0.368 Crohn Disease T300A variant of autophagy ATG16L1 gene is associated with decreased antigen sam... BeFree 24022642 Detail
0.033 ulcerative colitis We confirm the strong association between T300A and CD, specifically ileal subph... BeFree 18671817 Detail
0.368 Crohn Disease Genome-wide association study identifies new susceptibility loci for Crohn disea... GWASCAT 17435756 Detail
0.173 Inflammatory Bowel Diseases IL23R R381Q and ATG16L1 T300A are strongly associated with Crohn's disease in a ... BeFree 17894849 Detail
0.234 ulcerative colitis One hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 u... BeFree 20082483 Detail
0.560 Crohn Disease One hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 u... BeFree 20082483 Detail
0.371 Crohn Disease IL23R R381Q and ATG16L1 T300A are strongly associated with Crohn's disease in a ... BeFree 17894849 Detail
0.368 Crohn Disease One hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 u... BeFree 20082483 Detail
0.397 Inflammatory Bowel Diseases rs11209026 and rs2241880 genotype distributions were examined both within IBD cl... BeFree 17894849 Detail
0.368 Crohn Disease IL23R R381Q and ATG16L1 T300A are strongly associated with Crohn's disease in a ... BeFree 17894849 Detail
0.033 ulcerative colitis One hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 u... BeFree 20082483 Detail
0.371 Crohn Disease One hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 u... BeFree 20082483 Detail
0.340 Inflammatory Bowel Diseases IL23R R381Q and ATG16L1 T300A are strongly associated with Crohn's disease in a ... BeFree 17894849 Detail
0.327 ulcerative colitis One hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 u... BeFree 20082483 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_030803.7(ATG16L1):c.898A>G (p.Thr300Ala) AND Inflammatory bowel disease 10, susceptibility to ClinVar Detail
NM_030803.7(ATG16L1):c.898A>G (p.Thr300Ala) AND not specified ClinVar Detail
NM_030803.7(ATG16L1):c.898A>G (p.Thr300Ala) AND ATG16L1-related disorder ClinVar Detail
Prior to multiple testing correction, univariate analysis associated APOE rs429358, rs7412 and ATG16... DisGeNET Detail
Prior to multiple testing correction, univariate analysis associated APOE rs429358, rs7412 and ATG16... DisGeNET Detail
Prior to multiple testing correction, univariate analysis associated APOE rs429358, rs7412 and ATG16... DisGeNET Detail
Detection of Mycobacterium avium subspecies paratuberculosis in patients with Crohn's disease is unr... DisGeNET Detail
Detection of Mycobacterium avium subspecies paratuberculosis in patients with Crohn's disease is unr... DisGeNET Detail
To investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autopha... DisGeNET Detail
To investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autopha... DisGeNET Detail
To investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autopha... DisGeNET Detail
To investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autopha... DisGeNET Detail
The aim of this study was to determine the role of the ATG16L1 (rs2241880) and IRGM (rs13361189 and ... DisGeNET Detail
The aim of this study was to determine the role of the ATG16L1 (rs2241880) and IRGM (rs13361189 and ... DisGeNET Detail
In conclusion, our results confirm the ATG16L1 rs2241880 and IRGM rs13361189 and rs4958847 polymorph... DisGeNET Detail
In conclusion, our results confirm the ATG16L1 rs2241880 and IRGM rs13361189 and rs4958847 polymorph... DisGeNET Detail
We confirmed a strong association between three NOD2/CARD15 gene variants (Pro268Ser, OR = 2.52, 95%... DisGeNET Detail
We confirmed a strong association between three NOD2/CARD15 gene variants (Pro268Ser, OR = 2.52, 95%... DisGeNET Detail
We confirmed a strong association between three NOD2/CARD15 gene variants (Pro268Ser, OR = 2.52, 95%... DisGeNET Detail
We confirmed a strong association between three NOD2/CARD15 gene variants (Pro268Ser, OR = 2.52, 95%... DisGeNET Detail
The ATG16L1 gene variants rs2241879 and rs2241880 (T300A) are strongly associated with susceptibilit... DisGeNET Detail
In addition, the carriage of T300A variant alleles conferred a protective effect in UC. DisGeNET Detail
However a possible role of ATG16L1 (T300A) on CD phenotype was suggested. DisGeNET Detail
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. DisGeNET Detail
Genome-wide association studies have described an association of the ATG16L1 (autophagy 16-like 1) g... DisGeNET Detail
The ATG16L1 T300A polymorphism contributes to susceptibility to CD and UC in adults, but different i... DisGeNET Detail
Our aims were: to replicate the ATG16L1 Thr300Ala association with inflammatory bowel disease (IBD) ... DisGeNET Detail
We found a statistically significant interaction with respect to Crohn disease risk between rs224188... DisGeNET Detail
Publications addressing the relationship between rs2241880/T300A polymorphism of ATG16L1 and Crohn's... DisGeNET Detail
Thr300Ala polymorphism in ATG16L1 was reported as a susceptibility factor to Crohn's disease (CD). DisGeNET Detail
With respect to ATG16L1, the G allele of SNP rs2241880 has been shown in multiple association studie... DisGeNET Detail
Our aims were: to replicate the ATG16L1 Thr300Ala association with inflammatory bowel disease (IBD) ... DisGeNET Detail
T300A polymorphism of ATG16L1 and susceptibility to inflammatory bowel diseases: a meta-analysis. DisGeNET Detail
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. DisGeNET Detail
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates au... DisGeNET Detail
ATG16L1 T300A polymorphism and Crohn's disease susceptibility: evidence from 13,022 cases and 17,532... DisGeNET Detail
ATG16L1 T300A shows strong associations with disease subgroups in a large Australian IBD population:... DisGeNET Detail
ATG16L1 T300A shows strong associations with disease subgroups in a large Australian IBD population:... DisGeNET Detail
Role of ATG16L1 Thr300Ala polymorphism in inflammatory bowel disease: a Study in the Spanish populat... DisGeNET Detail
T300A variant of autophagy ATG16L1 gene is associated with decreased antigen sampling and processing... DisGeNET Detail
We confirm the strong association between T300A and CD, specifically ileal subphenotype, and also re... DisGeNET Detail
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates au... DisGeNET Detail
IL23R R381Q and ATG16L1 T300A are strongly associated with Crohn's disease in a study of New Zealand... DisGeNET Detail
One hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (U... DisGeNET Detail
One hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (U... DisGeNET Detail
IL23R R381Q and ATG16L1 T300A are strongly associated with Crohn's disease in a study of New Zealand... DisGeNET Detail
One hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (U... DisGeNET Detail
rs11209026 and rs2241880 genotype distributions were examined both within IBD clinical subphenotypes... DisGeNET Detail
IL23R R381Q and ATG16L1 T300A are strongly associated with Crohn's disease in a study of New Zealand... DisGeNET Detail
One hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (U... DisGeNET Detail
One hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (U... DisGeNET Detail
IL23R R381Q and ATG16L1 T300A are strongly associated with Crohn's disease in a study of New Zealand... DisGeNET Detail
One hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (U... DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs2241880 dbSNP
Genome
hg19
Position
chr2:234,183,368-234,183,368
Variant Type
snv
Reference Allele
A
Alternative Allele
G
Filtering Status (HGVD)
PASS
# of samples (HGVD)
847
Mean of sample read depth (HGVD)
10.94
Standard deviation of sample read depth (HGVD)
15.77
Number of reference allele (HGVD)
1278
Number of alternative allele (HGVD)
416
Allele Frequency (HGVD)
0.24557260920897284
Gene Symbol (HGVD)
ATG16L1
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs2241880
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.22
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
3687
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
East Asian Chromosome Counts (ExAC)
8628
East Asian Allele Counts (ExAC)
2873
East Asian Heterozygous Counts (ExAC)
1945
East Asian Homozygous Counts (ExAC)
464
East Asian Allele Frequency (ExAC)
0.33298562818729716
Chromosome Counts in All Race (ExAC)
121220
Allele Counts in All Race (ExAC)
55495
Heterozygous Counts in All Race (ExAC)
28325
Homozygous Counts in All Race (ExAC)
13585
Allele Frequency in All Race (ExAC)
0.45780399274047184
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