Have questions? Visit https://www.reddit.com/r/SNPedia

rs1085093

From SNPedia

Orientationplus
Stabilizedplus
Make rs1085093(C;C)
Make rs1085093(C;T)
Make rs1085093(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position84295665
GeneLOC101927633
is asnp
is mentioned by
dbSNPrs1085093
ebirs1085093
HLIrs1085093
Exacrs1085093
Varsomers1085093
Maprs1085093
PheGenIrs1085093
hapmaprs1085093
1000 genomesrs1085093
hgdprs1085093
ensemblrs1085093
gopubmedrs1085093
geneviewrs1085093
scholarrs1085093
googlers1085093
pharmgkbrs1085093
gwascentralrs1085093
openSNPrs1085093
23andMers1085093
23andMe allrs1085093
SNP Nexus

SNPshotrs1085093
SNPdbers1085093
MSV3drs1085093
GWAS Ctlgrs1085093
GMAF0.1598
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20694148OA-icon.png]
Trait
Title A genome-wide association study of the metabolic syndrome in Indian Asian men
Risk Allele
P-val 0.000003
Odds Ratio None None