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rs2681472

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0
Make rs2681472(C;C)
Make rs2681472(C;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position89615182
GeneATP2B1
is asnp
is mentioned by
dbSNPrs2681472
ebirs2681472
HLIrs2681472
Exacrs2681472
Varsomers2681472
Maprs2681472
PheGenIrs2681472
hapmaprs2681472
1000 genomesrs2681472
hgdprs2681472
ensemblrs2681472
gopubmedrs2681472
geneviewrs2681472
scholarrs2681472
googlers2681472
pharmgkbrs2681472
gwascentralrs2681472
openSNPrs2681472
23andMers2681472
23andMe allrs2681472
SNP Nexus

SNPshotrs2681472
SNPdbers2681472
MSV3drs2681472
GWAS Ctlgrs2681472
GMAF0.1924
Max Magnitude0
? (C;C) (C;T) (T;T) 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 1E-9
Odds Ratio 0.50 [0.34-0.66] mm Hg increase


[PMID 22229515] Polymorphism near the ATP2B1 gene is associated with hypertension risk in East Asians: A meta-analysis involving 15 909 cases and 18 529 controls


[PMID 21228780] Novel genetic variations associated with salt sensitivity in the Korean population.


GET Evidence
rs2681472
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.25
summary



[PMID 23036851] Treatment factors rather than genetic variation determine metabolic syndrome in childhood cancer survivors


[PMID 23079715] Common variants in the ATP2B1 gene are associated with hypertension and arterial stiffness in Chinese population.