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rs199473334

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473334(A;A)
Make rs199473334(A;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38550443
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473334
ebirs199473334
HLIrs199473334
Exacrs199473334
Varsomers199473334
Maprs199473334
PheGenIrs199473334
hapmaprs199473334
1000 genomesrs199473334
hgdprs199473334
ensemblrs199473334
gopubmedrs199473334
geneviewrs199473334
scholarrs199473334
googlers199473334
pharmgkbrs199473334
gwascentralrs199473334
openSNPrs199473334
23andMers199473334
23andMe allrs199473334
SNP Nexus

SNPshotrs199473334
SNPdbers199473334
MSV3drs199473334
GWAS Ctlgrs199473334
Max Magnitude0
ClinVar
Risk rs199473334(A;A)
Alt rs199473334(A;A)
Reference rs199473334(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38591934A>T
CLNSRC ClinVar
CLNACC RCV000058817.2,