rs3790844
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 2 | reduced risk (0.59x) of pancreatic cancer |
(C;T) | 1.5 | slightly reduced risk (0.77x) for pancreatic cancer |
(T;T) | 0 | common/normal |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 200038304 |
Gene | NR5A2 |
is a | snp |
is | mentioned by |
dbSNP | rs3790844 |
dbSNP (classic) | rs3790844 |
ClinGen | rs3790844 |
ebi | rs3790844 |
HLI | rs3790844 |
Exac | rs3790844 |
Gnomad | rs3790844 |
Varsome | rs3790844 |
LitVar | rs3790844 |
Map | rs3790844 |
PheGenI | rs3790844 |
Biobank | rs3790844 |
1000 genomes | rs3790844 |
hgdp | rs3790844 |
ensembl | rs3790844 |
geneview | rs3790844 |
scholar | rs3790844 |
rs3790844 | |
pharmgkb | rs3790844 |
gwascentral | rs3790844 |
openSNP | rs3790844 |
23andMe | rs3790844 |
SNPshot | rs3790844 |
SNPdbe | rs3790844 |
MSV3d | rs3790844 |
GWAS Ctlg | rs3790844 |
GMAF | 0.3453 |
Max Magnitude | 2 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
This SNP has been recognized by the Coriell Personalized Medicine Collaborative ICOB.
|
GWAS snp | |
---|---|
PMID | [PMID 20101243] |
Trait | Pancreatic cancer |
Title | A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33 |
Risk Allele | T |
P-val | 2E-10 |
Odds Ratio | 1.30 [1.19-1.41] |
23andMe reports that the G allele of this SNP appears to lower the risk of pancreatic cancer. [PMID 20101243]
[PMID 20686608] Genome-wide association study of pancreatic cancer in Japanese population.