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rs16879765

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs16879765(C;T)
Make rs16879765(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position37949493
GeneEPDR1
is asnp
is mentioned by
dbSNPrs16879765
dbSNP (old)rs16879765
ClinGenrs16879765
ebirs16879765
HLIrs16879765
Exacrs16879765
Varsomers16879765
Maprs16879765
PheGenIrs16879765
Biobankrs16879765
1000 genomesrs16879765
hgdprs16879765
ensemblrs16879765
gopubmedrs16879765
geneviewrs16879765
scholarrs16879765
googlers16879765
pharmgkbrs16879765
gwascentralrs16879765
openSNPrs16879765
23andMers16879765
23andMe allrs16879765
SNP Nexus

SNPshotrs16879765
SNPdbers16879765
MSV3drs16879765
GWAS Ctlgrs16879765
GMAF0.124
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21732829]
Trait
Title Wnt signaling and Dupuytren's disease.
Risk Allele A
P-val 6E-39
Odds Ratio 1.9800 None


[PMID 24089297] Common variants of the EPDR1 gene and the risk of Dupuytren's disease