chr1:113872746:G>C Detail (hg38) (PTPN22, AP4B1-AS1)

Information

Genome

Assembly Position
hg19 chr1:114,415,368-114,415,368 View the variant detail on this assembly version.
hg38 chr1:113,872,746-113,872,746

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.415
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[No Data.]

Prediction

ClinVar

Clinical Significance risk factor
Review star
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
risk factor 2006-03-15 no assertion criteria provided Diabetes mellitus, insulin-dependent, susceptibility to germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.226 Autoimmune Diseases Polymorphisms in PTPN22 are associated with many autoimmune diseases; while rs24... BeFree 22197427 Detail
0.475 Diabetes Mellitus, Insulin-Dependent Association of the PTPN22 gene (+1858C/T, -1123G/C) polymorphisms with type 1 di... BeFree 22572103 Detail
0.009 ulcerative colitis Association of PTPN22 gene (rs2488457) polymorphism with ulcerative colitis and ... BeFree 23456301 Detail
0.019 Juvenile arthritis STAT4 rs7574865 G/T and PTPN22 rs2488457 G/C polymorphisms influence the risk of... BeFree 25781893 Detail
0.004 juvenile rheumatoid arthritis STAT4 rs7574865 G/T and PTPN22 rs2488457 G/C polymorphisms influence the risk of... BeFree 25781893 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_015967.6(PTPN22):c.-1123C>G AND Diabetes mellitus, insulin-dependent, susceptibility to ClinVar Detail
Polymorphisms in PTPN22 are associated with many autoimmune diseases; while rs2476601 is supposed to... DisGeNET Detail
Association of the PTPN22 gene (+1858C/T, -1123G/C) polymorphisms with type 1 diabetes mellitus: a s... DisGeNET Detail
Association of PTPN22 gene (rs2488457) polymorphism with ulcerative colitis and high levels of PTPN2... DisGeNET Detail
STAT4 rs7574865 G/T and PTPN22 rs2488457 G/C polymorphisms influence the risk of developing juvenile... DisGeNET Detail
STAT4 rs7574865 G/T and PTPN22 rs2488457 G/C polymorphisms influence the risk of developing juvenile... DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs2488457 dbSNP
Genome
hg38
Position
chr1:113,872,746-113,872,746
Variant Type
snv
Reference Allele
G
Alternative Allele
C
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))
rs2488457
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.4148
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
6952
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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