Have questions? Visit https://www.reddit.com/r/SNPedia

rs4265793

From SNPedia

Orientationplus
Stabilizedplus
Make rs4265793(C;C)
Make rs4265793(C;T)
Make rs4265793(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position19017227
GeneTMC7
is asnp
is mentioned by
dbSNPrs4265793
ebirs4265793
HLIrs4265793
Exacrs4265793
Varsomers4265793
Maprs4265793
PheGenIrs4265793
hapmaprs4265793
1000 genomesrs4265793
hgdprs4265793
ensemblrs4265793
gopubmedrs4265793
geneviewrs4265793
scholarrs4265793
googlers4265793
pharmgkbrs4265793
gwascentralrs4265793
openSNPrs4265793
23andMers4265793
23andMe allrs4265793
SNP Nexus

SNPshotrs4265793
SNPdbers4265793
MSV3drs4265793
GWAS Ctlgrs4265793
GMAF0.09734
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 T
P-val 0.000006
Odds Ratio 1.2200 None