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rs4725982

From SNPedia

Orientationplus
Stabilizedplus
Make rs4725982(C;C)
Make rs4725982(C;T)
Make rs4725982(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position150940775
is asnp
is mentioned by
dbSNPrs4725982
ebirs4725982
HLIrs4725982
Exacrs4725982
Varsomers4725982
Maprs4725982
PheGenIrs4725982
hapmaprs4725982
1000 genomesrs4725982
hgdprs4725982
ensemblrs4725982
gopubmedrs4725982
geneviewrs4725982
scholarrs4725982
googlers4725982
pharmgkbrs4725982
gwascentralrs4725982
openSNPrs4725982
23andMers4725982
23andMe allrs4725982
SNP Nexus

SNPshotrs4725982
SNPdbers4725982
MSV3drs4725982
GWAS Ctlgrs4725982
GMAF0.3682
Max Magnitude
? (C;C) (C;T) (T;T) 28

23andMe blog Influences QT interval

GWAS snp
PMID [PMID 19305408OA-icon.png]
Trait QT interval
Title Common variants at ten loci influence QT interval duation in the QTGEN Study
Risk Allele T
P-val 5E-16
Odds Ratio 1.58 [1.23-1.92] msec increase


GWAS snp
PMID [PMID 20062061]
Trait Electrocardiographic traits
Title Genetic variation in SCN10A influences cardiac conduction
Risk Allele A
P-val 0.000003
Odds Ratio 2.08 [1.20-2.96] ms increase


GET Evidence
rs4725982
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.289062
summary



[PMID 26600494] Analysis of SNP (single nucleotide polymorphism) multiplex markers related to sudden cardiac death in Brazilian families