rs16879765

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics
(C;T)	2	Somewhat higher (~2x) risk for Dupuytren's Disease
(T;T)	3	Somewhat higher (~3x) risk for Dupuytren's Disease

Reference

GRCh38 38.1/141

Chromosome

7

Position

37949493

Gene

EPDR1

is a	snp
is	mentioned by
dbSNP	rs16879765
dbSNP (classic)	rs16879765
ClinGen	rs16879765
ebi	rs16879765
HLI	rs16879765
Exac	rs16879765
Gnomad	rs16879765
Varsome	rs16879765
LitVar	rs16879765
Map	rs16879765
PheGenI	rs16879765
Biobank	rs16879765
1000 genomes	rs16879765
hgdp	rs16879765
ensembl	rs16879765
geneview	rs16879765
scholar	rs16879765
google	rs16879765
pharmgkb	rs16879765
gwascentral	rs16879765
openSNP	rs16879765
23andMe	rs16879765
SNPshot	rs16879765
SNPdbe	rs16879765
MSV3d	rs16879765
GWAS Ctlg	rs16879765

GMAF

0.124

Max Magnitude

3

?	(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