rs7922612
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7922612(C;C) |
Make rs7922612(C;T) |
Make rs7922612(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 94051682 |
Gene | PLCE1 |
is a | snp |
is | mentioned by |
dbSNP | rs7922612 |
dbSNP (classic) | rs7922612 |
ClinGen | rs7922612 |
ebi | rs7922612 |
HLI | rs7922612 |
Exac | rs7922612 |
Gnomad | rs7922612 |
Varsome | rs7922612 |
LitVar | rs7922612 |
Map | rs7922612 |
PheGenI | rs7922612 |
Biobank | rs7922612 |
1000 genomes | rs7922612 |
hgdp | rs7922612 |
ensembl | rs7922612 |
geneview | rs7922612 |
scholar | rs7922612 |
rs7922612 | |
pharmgkb | rs7922612 |
gwascentral | rs7922612 |
openSNP | rs7922612 |
23andMe | rs7922612 |
SNPshot | rs7922612 |
SNPdbe | rs7922612 |
MSV3d | rs7922612 |
GWAS Ctlg | rs7922612 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24863943] A multigenic approach to evaluate genetic variants of PLCE1, LXRs, MMPs, TIMP, and CYP genes in gallbladder cancer predisposition
[PMID 24935391] Phospholipase C Epsilon 1 (PLCE1 rs2274223A>G, rs3765524C>T and rs7922612C>T) Polymorphisms and Esophageal Cancer Risk in the Kashmir Valley
[PMID 25139097] Role of novel and GWAS originated PLCE1 genetic variants in susceptibility and prognosis of esophageal cancer patients in northern Indian population