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rs8124695

From SNPedia

Orientationplus
Stabilizedplus
Make rs8124695(A;A)
Make rs8124695(A;C)
Make rs8124695(C;C)
ReferenceGRCh38 38.1/141
Chromosome20
Position40399796
is asnp
is mentioned by
dbSNPrs8124695
dbSNP (old)rs8124695
ClinGenrs8124695
ebirs8124695
HLIrs8124695
Exacrs8124695
Varsomers8124695
Maprs8124695
PheGenIrs8124695
Biobankrs8124695
1000 genomesrs8124695
hgdprs8124695
ensemblrs8124695
gopubmedrs8124695
geneviewrs8124695
scholarrs8124695
googlers8124695
pharmgkbrs8124695
gwascentralrs8124695
openSNPrs8124695
23andMers8124695
23andMe allrs8124695
SNP Nexus

SNPshotrs8124695
SNPdbers8124695
MSV3drs8124695
GWAS Ctlgrs8124695
GMAF0.1042
Max Magnitude
? (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