rs12615966
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12615966(C;C) |
Make rs12615966(C;T) |
Make rs12615966(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 104762499 |
is a | snp |
is | mentioned by |
dbSNP | rs12615966 |
dbSNP (classic) | rs12615966 |
ClinGen | rs12615966 |
ebi | rs12615966 |
HLI | rs12615966 |
Exac | rs12615966 |
Gnomad | rs12615966 |
Varsome | rs12615966 |
LitVar | rs12615966 |
Map | rs12615966 |
PheGenI | rs12615966 |
Biobank | rs12615966 |
1000 genomes | rs12615966 |
hgdp | rs12615966 |
ensembl | rs12615966 |
geneview | rs12615966 |
scholar | rs12615966 |
rs12615966 | |
pharmgkb | rs12615966 |
gwascentral | rs12615966 |
openSNP | rs12615966 |
23andMe | rs12615966 |
SNPshot | rs12615966 |
SNPdbe | rs12615966 |
MSV3d | rs12615966 |
GWAS Ctlg | rs12615966 |
GMAF | 0.1309 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20686608] |
Trait | |
Title | Genome-wide association study of pancreatic cancer in Japanese population |
Risk Allele | A |
P-val | 0.000007 |
Odds Ratio | 3.15 [1.91-5.21] |