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rs45589741

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs45589741(C;C)
Make rs45589741(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38566501
GeneSCN5A
is asnp
is mentioned by
dbSNPrs45589741
ebirs45589741
HLIrs45589741
Exacrs45589741
Varsomers45589741
Maprs45589741
PheGenIrs45589741
hapmaprs45589741
1000 genomesrs45589741
hgdprs45589741
ensemblrs45589741
gopubmedrs45589741
geneviewrs45589741
scholarrs45589741
googlers45589741
pharmgkbrs45589741
gwascentralrs45589741
openSNPrs45589741
23andMers45589741
23andMe allrs45589741
SNP Nexus

SNPshotrs45589741
SNPdbers45589741
MSV3drs45589741
GWAS Ctlgrs45589741
Max Magnitude0


ClinVar
Risk rs45589741(C;C)
Alt rs45589741(C;C)
Reference rs45589741(T;T)
Significance Pathogenic
Disease Acquired long QT syndrome
Variation info
Gene SCN5A
CLNDBN Acquired long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38607992A>G
CLNSRC ClinVar
CLNACC RCV000058598.2,