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rs4932194

From SNPedia

Orientationplus
Stabilizedplus
Make rs4932194(A;A)
Make rs4932194(A;C)
Make rs4932194(C;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position88702008
is asnp
is mentioned by
dbSNPrs4932194
dbSNP (old)rs4932194
ClinGenrs4932194
ebirs4932194
HLIrs4932194
Exacrs4932194
Varsomers4932194
Maprs4932194
PheGenIrs4932194
Biobankrs4932194
1000 genomesrs4932194
hgdprs4932194
ensemblrs4932194
gopubmedrs4932194
geneviewrs4932194
scholarrs4932194
googlers4932194
pharmgkbrs4932194
gwascentralrs4932194
openSNPrs4932194
23andMers4932194
23andMe allrs4932194
SNP Nexus

SNPshotrs4932194
SNPdbers4932194
MSV3drs4932194
GWAS Ctlgrs4932194
GMAF0.3398
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21732829]
Trait
Title Wnt signaling and Dupuytren's disease.
Risk Allele
P-val 8E-7
Odds Ratio 1.2200 None