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rs11775334

From SNPedia

Orientationplus
Stabilizedplus
Make rs11775334(A;A)
Make rs11775334(A;G)
Make rs11775334(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position10214110
GeneMSRA
is asnp
is mentioned by
dbSNPrs11775334
ebirs11775334
HLIrs11775334
Exacrs11775334
Varsomers11775334
Maprs11775334
PheGenIrs11775334
hapmaprs11775334
1000 genomesrs11775334
hgdprs11775334
ensemblrs11775334
gopubmedrs11775334
geneviewrs11775334
scholarrs11775334
googlers11775334
pharmgkbrs11775334
gwascentralrs11775334
openSNPrs11775334
23andMers11775334
23andMe allrs11775334
SNP Nexus

SNPshotrs11775334
SNPdbers11775334
MSV3drs11775334
GWAS Ctlgrs11775334
GMAF0.4541
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19430479OA-icon.png]
Trait Hypertension
Title Genome-wide association study of blood pressure and hypertension
Risk Allele A
P-val 0.000004
Odds Ratio 0.08 [0.04-0.12] increase in log odds


GET Evidence
rs11775334
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.5625
summary