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rs4789939

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs4789939(A;A)
Make rs4789939(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position78885621
GeneTIMP2
is asnp
is mentioned by
dbSNPrs4789939
ebirs4789939
HLIrs4789939
Exacrs4789939
Varsomers4789939
Maprs4789939
PheGenIrs4789939
hapmaprs4789939
1000 genomesrs4789939
hgdprs4789939
ensemblrs4789939
gopubmedrs4789939
geneviewrs4789939
scholarrs4789939
googlers4789939
pharmgkbrs4789939
gwascentralrs4789939
openSNPrs4789939
23andMers4789939
23andMe allrs4789939
SNP Nexus

SNPshotrs4789939
SNPdbers4789939
MSV3drs4789939
GWAS Ctlgrs4789939
GMAF0.3053
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21732829]
Trait
Title Wnt signaling and Dupuytren's disease.
Risk Allele
P-val 6E-7
Odds Ratio 1.2200 None