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rs1805126

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1805126(C;C)
Make rs1805126(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position38550915
GeneSCN5A
is asnp
is mentioned by
dbSNPrs1805126
ebirs1805126
HLIrs1805126
Exacrs1805126
Varsomers1805126
Maprs1805126
PheGenIrs1805126
hapmaprs1805126
1000 genomesrs1805126
hgdprs1805126
ensemblrs1805126
gopubmedrs1805126
geneviewrs1805126
scholarrs1805126
googlers1805126
pharmgkbrs1805126
gwascentralrs1805126
openSNPrs1805126
23andMers1805126
23andMe allrs1805126
SNP Nexus

SNPshotrs1805126
SNPdbers1805126
MSV3drs1805126
GWAS Ctlgrs1805126
GMAF0.4936
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23463857OA-icon.png]
Trait Electrocardiographic conduction measures
Title Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.
Risk Allele A
P-val 3E-20
Odds Ratio .66 [NR] msec decrease


[PMID 17534376OA-icon.png] Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjects.


[PMID 18368697] SCN5A variants in Japanese patients with left ventricular noncompaction and arrhythmia.


ClinVar
Risk rs1805126(C;C)
Alt rs1805126(C;C)
Reference rs1805126(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene SCN5A
CLNDBN not specified
Reversed 1
HGVS NC_000003.11:g.38592406A>G
CLNSRC ClinVar GeneDx
CLNACC RCV000041627.4,