chr11:71456403:G>T Detail (hg38) (NADSYN1)

Information

Genome

Assembly Position
hg19 chr11:71,167,449-71,167,449 View the variant detail on this assembly version.
hg38 chr11:71,456,403-71,456,403

HGVS

Type Transcript Protein
RefSeq NM_018161.4:c.146+1233G>T
Ensemble ENST00000319023.7:c.146+1233G>T
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.326
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 608285 OMIM
HGNC 29832 HGNC
Ensembl ENSG00000172890 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv43108146 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.022 Diabetes Mellitus, Insulin-Dependent DHCR7/NADSYN1 rs12785878 and CYP27B1 rs4646536 may play an important role in isl... BeFree 23979957 Detail
<0.001 Coronary heart disease Effect of polymorphisms in the NADSYN1/DHCR7 locus (rs12785878 and rs1790349) on... BeFree 24642724 Detail
<0.001 coronary artery disease Effect of polymorphisms in the NADSYN1/DHCR7 locus (rs12785878 and rs1790349) on... BeFree 24642724 Detail
<0.001 Cardiovascular Diseases Recent genome-wide association studies have identified the rs1790349 and rs12785... BeFree 24642724 Detail
<0.001 Coronary Arteriosclerosis Effect of polymorphisms in the NADSYN1/DHCR7 locus (rs12785878 and rs1790349) on... BeFree 24642724 Detail
<0.001 Coronary heart disease Effect of polymorphisms in the NADSYN1/DHCR7 locus (rs12785878 and rs1790349) on... BeFree 24642724 Detail
<0.001 Coronary Arteriosclerosis Effect of polymorphisms in the NADSYN1/DHCR7 locus (rs12785878 and rs1790349) on... BeFree 24642724 Detail
<0.001 coronary artery disease Effect of polymorphisms in the NADSYN1/DHCR7 locus (rs12785878 and rs1790349) on... BeFree 24642724 Detail
<0.001 Cardiovascular Diseases Recent genome-wide association studies have identified the rs1790349 and rs12785... BeFree 24642724 Detail
<0.001 Diabetes Mellitus, Insulin-Dependent DHCR7/NADSYN1 rs12785878 and CYP27B1 rs4646536 may play an important role in isl... BeFree 23979957 Detail
<0.001 Diabetes Mellitus, Insulin-Dependent The second SNP, rs12785878, is located near DHCR7 (Chr11), a genetic determinant... BeFree 22130326 Detail
0.120 Vitamin D Deficiency Common genetic determinants of vitamin D insufficiency: a genome-wide associatio... GWASCAT 20541252 Detail
<0.001 Hepatitis C, Chronic The well-known associations between CYP2R1 (rs1993116, rs10741657), GC (rs228267... BeFree 23734184 Detail
<0.001 liver carcinoma The well-known associations between CYP2R1 (rs1993116, rs10741657), GC (rs228267... BeFree 23734184 Detail
<0.001 colon carcinoma In the present study, we investigated the association of three functional gene v... BeFree 23793229 Detail
<0.001 Hepatitis C, Chronic The well-known associations between CYP2R1 (rs1993116, rs10741657), GC (rs228267... BeFree 23734184 Detail
<0.001 Malignant tumor of colon In the present study, we investigated the association of three functional gene v... BeFree 23793229 Detail
<0.001 colon carcinoma In the present study, we investigated the association of three functional gene v... BeFree 23793229 Detail
<0.001 liver carcinoma The well-known associations between CYP2R1 (rs1993116, rs10741657), GC (rs228267... BeFree 23734184 Detail
<0.001 Malignant tumor of colon In the present study, we investigated the association of three functional gene v... BeFree 23793229 Detail
Annotation

Annotations

DescrptionSourceLinks
DHCR7/NADSYN1 rs12785878 and CYP27B1 rs4646536 may play an important role in islet autoimmunity, the... DisGeNET Detail
Effect of polymorphisms in the NADSYN1/DHCR7 locus (rs12785878 and rs1790349) on plasma 25-hydroxyvi... DisGeNET Detail
Effect of polymorphisms in the NADSYN1/DHCR7 locus (rs12785878 and rs1790349) on plasma 25-hydroxyvi... DisGeNET Detail
Recent genome-wide association studies have identified the rs1790349 and rs12785878 single-nucleotid... DisGeNET Detail
Effect of polymorphisms in the NADSYN1/DHCR7 locus (rs12785878 and rs1790349) on plasma 25-hydroxyvi... DisGeNET Detail
Effect of polymorphisms in the NADSYN1/DHCR7 locus (rs12785878 and rs1790349) on plasma 25-hydroxyvi... DisGeNET Detail
Effect of polymorphisms in the NADSYN1/DHCR7 locus (rs12785878 and rs1790349) on plasma 25-hydroxyvi... DisGeNET Detail
Effect of polymorphisms in the NADSYN1/DHCR7 locus (rs12785878 and rs1790349) on plasma 25-hydroxyvi... DisGeNET Detail
Recent genome-wide association studies have identified the rs1790349 and rs12785878 single-nucleotid... DisGeNET Detail
DHCR7/NADSYN1 rs12785878 and CYP27B1 rs4646536 may play an important role in islet autoimmunity, the... DisGeNET Detail
The second SNP, rs12785878, is located near DHCR7 (Chr11), a genetic determinant of vitamin D insuff... DisGeNET Detail
Common genetic determinants of vitamin D insufficiency: a genome-wide association study. DisGeNET Detail
The well-known associations between CYP2R1 (rs1993116, rs10741657), GC (rs2282679), and DHCR7 (rs794... DisGeNET Detail
The well-known associations between CYP2R1 (rs1993116, rs10741657), GC (rs2282679), and DHCR7 (rs794... DisGeNET Detail
In the present study, we investigated the association of three functional gene variants in GC (rs228... DisGeNET Detail
The well-known associations between CYP2R1 (rs1993116, rs10741657), GC (rs2282679), and DHCR7 (rs794... DisGeNET Detail
In the present study, we investigated the association of three functional gene variants in GC (rs228... DisGeNET Detail
In the present study, we investigated the association of three functional gene variants in GC (rs228... DisGeNET Detail
The well-known associations between CYP2R1 (rs1993116, rs10741657), GC (rs2282679), and DHCR7 (rs794... DisGeNET Detail
In the present study, we investigated the association of three functional gene variants in GC (rs228... DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs12785878 dbSNP
Genome
hg38
Position
chr11:71,456,403-71,456,403
Variant Type
snv
Reference Allele
G
Alternative Allele
T
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))
rs12785878
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.3259
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
5462
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16758
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