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rs379742

From SNPedia

Orientationminus
Stabilizedminus
Make rs379742(C;C)
Make rs379742(C;T)
Make rs379742(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position106250703
is asnp
is mentioned by
dbSNPrs379742
ebirs379742
HLIrs379742
Exacrs379742
Varsomers379742
Maprs379742
PheGenIrs379742
hapmaprs379742
1000 genomesrs379742
hgdprs379742
ensemblrs379742
gopubmedrs379742
geneviewrs379742
scholarrs379742
googlers379742
pharmgkbrs379742
gwascentralrs379742
openSNPrs379742
23andMers379742
23andMe allrs379742
SNP Nexus

SNPshotrs379742
SNPdbers379742
MSV3drs379742
GWAS Ctlgrs379742
GMAF0.2461
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23143602OA-icon.png]
Trait Pancreatitis
Title Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis.
Risk Allele T
P-val 6E-7
Odds Ratio 1.20 [1.10-1.30]