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rs1550576

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs1550576(C;T)
Make rs1550576(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position57921216
is asnp
is mentioned by
dbSNPrs1550576
ebirs1550576
HLIrs1550576
Exacrs1550576
Varsomers1550576
Maprs1550576
PheGenIrs1550576
hapmaprs1550576
1000 genomesrs1550576
hgdprs1550576
ensemblrs1550576
gopubmedrs1550576
geneviewrs1550576
scholarrs1550576
googlers1550576
pharmgkbrs1550576
gwascentralrs1550576
openSNPrs1550576
23andMers1550576
23andMe allrs1550576
SNP Nexus

SNPshotrs1550576
SNPdbers1550576
MSV3drs1550576
GWAS Ctlgrs1550576
GMAF0.1827
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19609347OA-icon.png]
Trait Hypertension
Title A Genome-Wide Association Study of Hypertension and Blood Pressure in African Americans
Risk Allele
P-val 0.000003
Odds Ratio 1.92 [NR]


GET Evidence
rs1550576
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.132812
summary