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rs3814231

From SNPedia

Orientationminus
Stabilizedminus
Make rs3814231(A;A)
Make rs3814231(A;G)
Make rs3814231(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position113721259
GeneCASP7
is asnp
is mentioned by
dbSNPrs3814231
ebirs3814231
HLIrs3814231
Exacrs3814231
Varsomers3814231
Maprs3814231
PheGenIrs3814231
hapmaprs3814231
1000 genomesrs3814231
hgdprs3814231
ensemblrs3814231
gopubmedrs3814231
geneviewrs3814231
scholarrs3814231
googlers3814231
pharmgkbrs3814231
gwascentralrs3814231
openSNPrs3814231
23andMers3814231
23andMe allrs3814231
SNP Nexus

SNPshotrs3814231
SNPdbers3814231
MSV3drs3814231
GWAS Ctlgrs3814231
GMAF0.2718
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 22548721] Association between CASP7 and CASP14 genetic polymorphisms and the risk of childhood leukemia

GWAS snp
PMID [PMID 22561518OA-icon.png]
Trait
Title Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.
Risk Allele G
P-val 4E-8
Odds Ratio 1.2300 None