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rs790123

From SNPedia

Orientationminus
Stabilizedminus
Make rs790123(A;A)
Make rs790123(A;G)
Make rs790123(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position122670146
is asnp
is mentioned by
dbSNPrs790123
dbSNP (classic)rs790123
ClinGenrs790123
ebirs790123
HLIrs790123
Exacrs790123
Gnomadrs790123
Varsomers790123
LitVarrs790123
Maprs790123
PheGenIrs790123
Biobankrs790123
1000 genomesrs790123
hgdprs790123
ensemblrs790123
geneviewrs790123
scholarrs790123
googlers790123
pharmgkbrs790123
gwascentralrs790123
openSNPrs790123
23andMers790123
SNPshotrs790123
SNPdbers790123
MSV3drs790123
GWAS Ctlgrs790123
GMAF0.4968
Max Magnitude0
? (A;A) (A;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 T
P-val 0.000006
Odds Ratio 1.0700 None