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rs10496166

From SNPedia

Orientationminus
Stabilizedminus
Make rs10496166(C;C)
Make rs10496166(C;T)
Make rs10496166(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position68836777
GeneLOC100996448
is asnp
is mentioned by
dbSNPrs10496166
ebirs10496166
HLIrs10496166
Exacrs10496166
Varsomers10496166
Maprs10496166
PheGenIrs10496166
hapmaprs10496166
1000 genomesrs10496166
hgdprs10496166
ensemblrs10496166
gopubmedrs10496166
geneviewrs10496166
scholarrs10496166
googlers10496166
pharmgkbrs10496166
gwascentralrs10496166
openSNPrs10496166
23andMers10496166
23andMe allrs10496166
SNP Nexus

SNPshotrs10496166
SNPdbers10496166
MSV3drs10496166
GWAS Ctlgrs10496166
GMAF0.3104
Max Magnitude
? (C;C) (C;T) (T;T) 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 0.000004
Odds Ratio 0.18 [0.10-0.26] unit increase


GET Evidence
rs10496166
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.304688
summary