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rs7865146

From SNPedia

Orientationplus
Stabilizedplus
Make rs7865146(C;C)
Make rs7865146(C;T)
Make rs7865146(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position127857358
is asnp
is mentioned by
dbSNPrs7865146
ebirs7865146
HLIrs7865146
Exacrs7865146
Varsomers7865146
Maprs7865146
PheGenIrs7865146
hapmaprs7865146
1000 genomesrs7865146
hgdprs7865146
ensemblrs7865146
gopubmedrs7865146
geneviewrs7865146
scholarrs7865146
googlers7865146
pharmgkbrs7865146
gwascentralrs7865146
openSNPrs7865146
23andMers7865146
23andMe allrs7865146
SNP Nexus

SNPshotrs7865146
SNPdbers7865146
MSV3drs7865146
GWAS Ctlgrs7865146
GMAF0.4229
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 A
P-val 0.000001
Odds Ratio 1.19 [0.71-1.67] mmHg decrease