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rs11110912

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 1.1 1.3x high blood pressure risk
(C;G) 1.1 1.3x high blood pressure risk
(G;G) normal
ReferenceGRCh38 38.1/141
Chromosome12
Position101648435
GeneLOC100505814, MYBPC1
is asnp
is mentioned by
dbSNPrs11110912
ebirs11110912
HLIrs11110912
Exacrs11110912
Varsomers11110912
Maprs11110912
PheGenIrs11110912
hapmaprs11110912
1000 genomesrs11110912
hgdprs11110912
ensemblrs11110912
gopubmedrs11110912
geneviewrs11110912
scholarrs11110912
googlers11110912
pharmgkbrs11110912
gwascentralrs11110912
openSNPrs11110912
23andMers11110912
23andMe allrs11110912
SNP Nexus

SNPshotrs11110912
SNPdbers11110912
MSV3drs11110912
GWAS Ctlgrs11110912
GMAF0.1061
Max Magnitude1.1
? (C;C) (C;G) (G;G) 28
rs11110912 has been reported in a large study to be associated with high blood pressure.

The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.33 (CI 1.18-1.51), and for homozygotes, 1.34 (CI 0.96-1.86). [PMID 17554300OA-icon.png]


[PMID 18523456OA-icon.png] Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program.