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rs13075436

From SNPedia

Orientationplus
Stabilizedplus
Make rs13075436(C;C)
Make rs13075436(C;T)
Make rs13075436(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position127242305
is asnp
is mentioned by
dbSNPrs13075436
ebirs13075436
HLIrs13075436
Exacrs13075436
Varsomers13075436
Maprs13075436
PheGenIrs13075436
hapmaprs13075436
1000 genomesrs13075436
hgdprs13075436
ensemblrs13075436
gopubmedrs13075436
geneviewrs13075436
scholarrs13075436
googlers13075436
pharmgkbrs13075436
gwascentralrs13075436
openSNPrs13075436
23andMers13075436
23andMe allrs13075436
SNP Nexus

SNPshotrs13075436
SNPdbers13075436
MSV3drs13075436
GWAS Ctlgrs13075436
GMAF0.2938
Max Magnitude
? (C;C) (C;T) (T;T) 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 0.000006
Odds Ratio 1.3000 None