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rs2384550

From SNPedia

Orientationplus
Stabilizedplus
Make rs2384550(A;A)
Make rs2384550(A;G)
Make rs2384550(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position114914926
is asnp
is mentioned by
dbSNPrs2384550
ebirs2384550
HLIrs2384550
Exacrs2384550
Varsomers2384550
Maprs2384550
PheGenIrs2384550
hapmaprs2384550
1000 genomesrs2384550
hgdprs2384550
ensemblrs2384550
gopubmedrs2384550
geneviewrs2384550
scholarrs2384550
googlers2384550
pharmgkbrs2384550
gwascentralrs2384550
openSNPrs2384550
23andMers2384550
23andMe allrs2384550
SNP Nexus

SNPshotrs2384550
SNPdbers2384550
MSV3drs2384550
GWAS Ctlgrs2384550
GMAF0.287
Max Magnitude
? (A;A) (A;G) (G;G) 28
23andMe blog blood pressure
GWAS snp
PMID [PMID 19430479OA-icon.png]
Trait Diastolic Blood Pressure
Title Genome-wide association study of blood pressure and hypertension
Risk Allele A
P-val 4E-8
Odds Ratio 0.35 [0.23-0.47] mm Hg decrease
GWAS snp
PMID [PMID 21909110OA-icon.png]
Trait
Title Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
Risk Allele G
P-val 0.000004
Odds Ratio 0.2270 [0.13-0.32] mmHg increase


GET Evidence
rs2384550
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.289062
summary