rs6711606
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6711606(G;G) |
Make rs6711606(G;T) |
Make rs6711606(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 101305708 |
Gene | RNF149 |
is a | snp |
is | mentioned by |
dbSNP | rs6711606 |
dbSNP (classic) | rs6711606 |
ClinGen | rs6711606 |
ebi | rs6711606 |
HLI | rs6711606 |
Exac | rs6711606 |
Gnomad | rs6711606 |
Varsome | rs6711606 |
LitVar | rs6711606 |
Map | rs6711606 |
PheGenI | rs6711606 |
Biobank | rs6711606 |
1000 genomes | rs6711606 |
hgdp | rs6711606 |
ensembl | rs6711606 |
geneview | rs6711606 |
scholar | rs6711606 |
rs6711606 | |
pharmgkb | rs6711606 |
gwascentral | rs6711606 |
openSNP | rs6711606 |
23andMe | rs6711606 |
SNPshot | rs6711606 |
SNPdbe | rs6711606 |
MSV3d | rs6711606 |
GWAS Ctlg | rs6711606 |
GMAF | 0.1074 |
Max Magnitude | 0 |
? | (G;G) (G;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 | 0.000004 |
Odds Ratio | 2.81 [1.81-4.37] |