rs8124695

Orientation

plus

Stabilized

plus

Make rs8124695(A;A)

Make rs8124695(A;C)

Make rs8124695(C;C)

Reference

GRCh38 38.1/141

Chromosome

20

Position

40399796

is a	snp
is	mentioned by
dbSNP	rs8124695
dbSNP (classic)	rs8124695
ClinGen	rs8124695
ebi	rs8124695
HLI	rs8124695
Exac	rs8124695
Gnomad	rs8124695
Varsome	rs8124695
LitVar	rs8124695
Map	rs8124695
PheGenI	rs8124695
Biobank	rs8124695
1000 genomes	rs8124695
hgdp	rs8124695
ensembl	rs8124695
geneview	rs8124695
scholar	rs8124695
google	rs8124695
pharmgkb	rs8124695
gwascentral	rs8124695
openSNP	rs8124695
23andMe	rs8124695
SNPshot	rs8124695
SNPdbe	rs8124695
MSV3d	rs8124695
GWAS Ctlg	rs8124695

GMAF

0.1042

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

GWAS snp
PMID	[PMID 21732829]
Trait
Title	Wnt signaling and Dupuytren's disease.
Risk Allele	A
P-val	8E-10
Odds Ratio	1.4800 None