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rs9791170

From SNPedia

Orientationplus
Stabilizedplus
Make rs9791170(C;C)
Make rs9791170(C;T)
Make rs9791170(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position132233934
is asnp
is mentioned by
dbSNPrs9791170
ebirs9791170
HLIrs9791170
Exacrs9791170
Varsomers9791170
Maprs9791170
PheGenIrs9791170
hapmaprs9791170
1000 genomesrs9791170
hgdprs9791170
ensemblrs9791170
gopubmedrs9791170
geneviewrs9791170
scholarrs9791170
googlers9791170
pharmgkbrs9791170
gwascentralrs9791170
openSNPrs9791170
23andMers9791170
23andMe allrs9791170
SNP Nexus

SNPshotrs9791170
SNPdbers9791170
MSV3drs9791170
GWAS Ctlgrs9791170
GMAF0.432
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19609347OA-icon.png] A genome-wide association study of hypertension and blood pressure in African Americans