Have questions? Visit https://www.reddit.com/r/SNPedia

rs2278952

From SNPedia

Orientationminus
Stabilizedminus
Make rs2278952(C;C)
Make rs2278952(C;T)
Make rs2278952(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position17582270
GenePEMT
is asnp
is mentioned by
dbSNPrs2278952
ebirs2278952
HLIrs2278952
Exacrs2278952
Varsomers2278952
Maprs2278952
PheGenIrs2278952
hapmaprs2278952
1000 genomesrs2278952
hgdprs2278952
ensemblrs2278952
gopubmedrs2278952
geneviewrs2278952
scholarrs2278952
googlers2278952
pharmgkbrs2278952
gwascentralrs2278952
openSNPrs2278952
23andMers2278952
23andMe allrs2278952
SNP Nexus

SNPshotrs2278952
SNPdbers2278952
MSV3drs2278952
GWAS Ctlgrs2278952
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 25759212] A distinct and replicable variant of the squamous cell carcinoma gene inositol polyphosphate-5-phosphatase modifies the susceptibility of arsenic-associated skin lesions in Bangladesh