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rs45609733

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45609733(C;T)
Make rs45609733(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38598998
GeneSCN5A
is asnp
is mentioned by
dbSNPrs45609733
ebirs45609733
HLIrs45609733
Exacrs45609733
Varsomers45609733
Maprs45609733
PheGenIrs45609733
hapmaprs45609733
1000 genomesrs45609733
hgdprs45609733
ensemblrs45609733
gopubmedrs45609733
geneviewrs45609733
scholarrs45609733
googlers45609733
pharmgkbrs45609733
gwascentralrs45609733
openSNPrs45609733
23andMers45609733
23andMe allrs45609733
SNP Nexus

SNPshotrs45609733
SNPdbers45609733
MSV3drs45609733
GWAS Ctlgrs45609733
Max Magnitude0


ClinVar
Risk rs45609733(T;T)
Alt rs45609733(T;T)
Reference rs45609733(C;C)
Significance Pathogenic
Disease not specified Congenital long QT syndrome not provided
Variation info
Gene SCN5A
CLNDBN not specified Congenital long QT syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38640489G>A
CLNSRC ClinVar
CLNACC RCV000041607.2, RCV000058466.2, RCV000225740.1,