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rs2717128

From SNPedia

Orientationminus
Stabilizedminus
Make rs2717128(C;C)
Make rs2717128(C;T)
Make rs2717128(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position77275676
is asnp
is mentioned by
dbSNPrs2717128
ebirs2717128
HLIrs2717128
Exacrs2717128
Varsomers2717128
Maprs2717128
PheGenIrs2717128
hapmaprs2717128
1000 genomesrs2717128
hgdprs2717128
ensemblrs2717128
gopubmedrs2717128
geneviewrs2717128
scholarrs2717128
googlers2717128
pharmgkbrs2717128
gwascentralrs2717128
openSNPrs2717128
23andMers2717128
23andMe allrs2717128
SNP Nexus

SNPshotrs2717128
SNPdbers2717128
MSV3drs2717128
GWAS Ctlgrs2717128
GMAF0.1474
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 G
P-val 0.000001
Odds Ratio 0.19 [0.11-0.27] unit decrease


GET Evidence
rs2717128
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.134921
summary