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rs7601713

From SNPedia

Orientationplus
Stabilizedplus
Make rs7601713(A;A)
Make rs7601713(A;C)
Make rs7601713(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position156696348
is asnp
is mentioned by
dbSNPrs7601713
ebirs7601713
HLIrs7601713
Exacrs7601713
Varsomers7601713
Maprs7601713
PheGenIrs7601713
hapmaprs7601713
1000 genomesrs7601713
hgdprs7601713
ensemblrs7601713
gopubmedrs7601713
geneviewrs7601713
scholarrs7601713
googlers7601713
pharmgkbrs7601713
gwascentralrs7601713
openSNPrs7601713
23andMers7601713
23andMe allrs7601713
SNP Nexus

SNPshotrs7601713
SNPdbers7601713
MSV3drs7601713
GWAS Ctlgrs7601713
GMAF0.1974
Max Magnitude
? (A;A) (A;C) (C;C) 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 A
P-val 0.000002
Odds Ratio 0.16 [0.10-0.22] unit decrease


GET Evidence
rs7601713
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.81746
summary