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rs11953630

From SNPedia

Orientationplus
Stabilizedplus
Make rs11953630(C;C)
Make rs11953630(C;T)
Make rs11953630(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position158418394
is asnp
is mentioned by
dbSNPrs11953630
ebirs11953630
HLIrs11953630
Exacrs11953630
Varsomers11953630
Maprs11953630
PheGenIrs11953630
hapmaprs11953630
1000 genomesrs11953630
hgdprs11953630
ensemblrs11953630
gopubmedrs11953630
geneviewrs11953630
scholarrs11953630
googlers11953630
pharmgkbrs11953630
gwascentralrs11953630
openSNPrs11953630
23andMers11953630
23andMe allrs11953630
SNP Nexus

SNPshotrs11953630
SNPdbers11953630
MSV3drs11953630
GWAS Ctlgrs11953630
GMAF0.2163
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21909115OA-icon.png]
Trait
Title Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Risk Allele T
P-val 2E-7
Odds Ratio 0.0520 [NR] % decrease
[PMID 22504314OA-icon.png] Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.