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rs2681492

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0
Make rs2681492(A;G)
Make rs2681492(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position89619312
GeneATP2B1
is asnp
is mentioned by
dbSNPrs2681492
ebirs2681492
HLIrs2681492
Exacrs2681492
Varsomers2681492
Maprs2681492
PheGenIrs2681492
hapmaprs2681492
1000 genomesrs2681492
hgdprs2681492
ensemblrs2681492
gopubmedrs2681492
geneviewrs2681492
scholarrs2681492
googlers2681492
pharmgkbrs2681492
gwascentralrs2681492
openSNPrs2681492
23andMers2681492
23andMe allrs2681492
SNP Nexus

SNPshotrs2681492
SNPdbers2681492
MSV3drs2681492
GWAS Ctlgrs2681492
GMAF0.2029
Max Magnitude0
? (A;A) (A;G) (G;G) 28

23andMe blog blood pressure

GWAS snp
PMID [PMID 19430479OA-icon.png]
Trait Systolic blood pressure
Title Genome-wide association study of blood pressure and hypertension
Risk Allele T
P-val 4E-11
Odds Ratio 0.85 [0.60-1.10] mm Hg increase


GET Evidence
rs2681492
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