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rs199473307

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473307(C;T)
Make rs199473307(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551091
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473307
ebirs199473307
HLIrs199473307
Exacrs199473307
Varsomers199473307
Maprs199473307
PheGenIrs199473307
hapmaprs199473307
1000 genomesrs199473307
hgdprs199473307
ensemblrs199473307
gopubmedrs199473307
geneviewrs199473307
scholarrs199473307
googlers199473307
pharmgkbrs199473307
gwascentralrs199473307
openSNPrs199473307
23andMers199473307
23andMe allrs199473307
SNP Nexus

SNPshotrs199473307
SNPdbers199473307
MSV3drs199473307
GWAS Ctlgrs199473307
Max Magnitude0
ClinVar
Risk rs199473307(T;T)
Alt rs199473307(T;T)
Reference rs199473307(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38592582G>A
CLNSRC ClinVar
CLNACC RCV000058758.2,