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rs7922612

From SNPedia

Orientationplus
Stabilizedplus
Make rs7922612(C;C)
Make rs7922612(C;T)
Make rs7922612(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position94051682
GenePLCE1
is asnp
is mentioned by
dbSNPrs7922612
ebirs7922612
HLIrs7922612
Exacrs7922612
Varsomers7922612
Maprs7922612
PheGenIrs7922612
hapmaprs7922612
1000 genomesrs7922612
hgdprs7922612
ensemblrs7922612
gopubmedrs7922612
geneviewrs7922612
scholarrs7922612
googlers7922612
pharmgkbrs7922612
gwascentralrs7922612
openSNPrs7922612
23andMers7922612
23andMe allrs7922612
SNP Nexus

SNPshotrs7922612
SNPdbers7922612
MSV3drs7922612
GWAS Ctlgrs7922612
Max Magnitude
? (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