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rs7168353

From SNPedia

Orientationplus
Stabilizedplus
Make rs7168353(C;C)
Make rs7168353(C;G)
Make rs7168353(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position93095172
GeneLOC101927025
is asnp
is mentioned by
dbSNPrs7168353
dbSNP (classic)rs7168353
ClinGenrs7168353
ebirs7168353
HLIrs7168353
Exacrs7168353
Gnomadrs7168353
Varsomers7168353
LitVarrs7168353
Maprs7168353
PheGenIrs7168353
Biobankrs7168353
1000 genomesrs7168353
hgdprs7168353
ensemblrs7168353
geneviewrs7168353
scholarrs7168353
googlers7168353
pharmgkbrs7168353
gwascentralrs7168353
openSNPrs7168353
23andMers7168353
SNPshotrs7168353
SNPdbers7168353
MSV3drs7168353
GWAS Ctlgrs7168353
GMAF0.1713
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GWAS snp
PMID [PMID 22566498OA-icon.png]
Trait
Title Genomic association analysis identifies multiple loci influencing antihypertensive response to an angiotensin II receptor blocker.
Risk Allele C
P-val 0.000001
Odds Ratio None None