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rs8015016

From SNPedia

Orientationplus
Stabilizedplus
Make rs8015016(A;A)
Make rs8015016(A;G)
Make rs8015016(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position95656071
GeneTCL6
is asnp
is mentioned by
dbSNPrs8015016
ebirs8015016
HLIrs8015016
Exacrs8015016
Varsomers8015016
Maprs8015016
PheGenIrs8015016
hapmaprs8015016
1000 genomesrs8015016
hgdprs8015016
ensemblrs8015016
gopubmedrs8015016
geneviewrs8015016
scholarrs8015016
googlers8015016
pharmgkbrs8015016
gwascentralrs8015016
openSNPrs8015016
23andMers8015016
23andMe allrs8015016
SNP Nexus

SNPshotrs8015016
SNPdbers8015016
MSV3drs8015016
GWAS Ctlgrs8015016
GMAF0.2392
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20031603OA-icon.png]
Trait QT interval
Title A Genome-Wide Association Scan of RR and QT Interval Duration in 3 European Genetically Isolated Populations: The EUROSPAN Project
Risk Allele G
P-val 5E-7
Odds Ratio 0.18 [0.10-0.26] unit decrease


GET Evidence
rs8015016
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.296875
summary