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rs12554086

From SNPedia

Orientationplus
Stabilizedplus
Make rs12554086(A;A)
Make rs12554086(A;G)
Make rs12554086(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position80192588
is asnp
is mentioned by
dbSNPrs12554086
ebirs12554086
HLIrs12554086
Exacrs12554086
Varsomers12554086
Maprs12554086
PheGenIrs12554086
hapmaprs12554086
1000 genomesrs12554086
hgdprs12554086
ensemblrs12554086
gopubmedrs12554086
geneviewrs12554086
scholarrs12554086
googlers12554086
pharmgkbrs12554086
gwascentralrs12554086
openSNPrs12554086
23andMers12554086
23andMe allrs12554086
SNP Nexus

SNPshotrs12554086
SNPdbers12554086
MSV3drs12554086
GWAS Ctlgrs12554086
GMAF0.2121
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20031603OA-icon.png]
Trait RR interval (heart rate)
Title A Genome-Wide Association Scan of RR and QT Interval Duration in 3 European Genetically Isolated Populations: The EUROSPAN Project
Risk Allele A
P-val 4E-7
Odds Ratio 0.16 [0.10-0.22] unit decrease


GET Evidence
rs12554086
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.145161
summary