rs12778749
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12778749(C;C) |
Make rs12778749(C;T) |
Make rs12778749(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 126158100 |
Gene | ADAM12 |
is a | snp |
is | mentioned by |
dbSNP | rs12778749 |
dbSNP (classic) | rs12778749 |
ClinGen | rs12778749 |
ebi | rs12778749 |
HLI | rs12778749 |
Exac | rs12778749 |
Gnomad | rs12778749 |
Varsome | rs12778749 |
LitVar | rs12778749 |
Map | rs12778749 |
PheGenI | rs12778749 |
Biobank | rs12778749 |
1000 genomes | rs12778749 |
hgdp | rs12778749 |
ensembl | rs12778749 |
geneview | rs12778749 |
scholar | rs12778749 |
rs12778749 | |
pharmgkb | rs12778749 |
gwascentral | rs12778749 |
openSNP | rs12778749 |
23andMe | rs12778749 |
SNPshot | rs12778749 |
SNPdbe | rs12778749 |
MSV3d | rs12778749 |
GWAS Ctlg | rs12778749 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24096698] |
Trait | Endometrial cancer |
Title | Genome-wide association study of endometrial cancer in E2C2. |
Risk Allele | |
P-val | 9E-6 |
Odds Ratio | NR NR |