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rs1206634

From SNPedia

Orientationminus
Stabilizedminus
Make rs1206634(A;A)
Make rs1206634(A;C)
Make rs1206634(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position96302380
is asnp
is mentioned by
dbSNPrs1206634
ebirs1206634
HLIrs1206634
Exacrs1206634
Varsomers1206634
Maprs1206634
PheGenIrs1206634
hapmaprs1206634
1000 genomesrs1206634
hgdprs1206634
ensemblrs1206634
gopubmedrs1206634
geneviewrs1206634
scholarrs1206634
googlers1206634
pharmgkbrs1206634
gwascentralrs1206634
openSNPrs1206634
23andMers1206634
23andMe allrs1206634
SNP Nexus

SNPshotrs1206634
SNPdbers1206634
MSV3drs1206634
GWAS Ctlgrs1206634
GMAF0.0532
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 23869418] Association Between a 11β-Hydroxysteroid Dehydrogenase Type 1 Gene Polymorphism and Metabolic Syndrome in a South Indian Population