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rs199473105

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473105(C;C)
Make rs199473105(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38606099
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473105
ebirs199473105
HLIrs199473105
Exacrs199473105
Varsomers199473105
Maprs199473105
PheGenIrs199473105
hapmaprs199473105
1000 genomesrs199473105
hgdprs199473105
ensemblrs199473105
gopubmedrs199473105
geneviewrs199473105
scholarrs199473105
googlers199473105
pharmgkbrs199473105
gwascentralrs199473105
openSNPrs199473105
23andMers199473105
23andMe allrs199473105
SNP Nexus

SNPshotrs199473105
SNPdbers199473105
MSV3drs199473105
GWAS Ctlgrs199473105
Max Magnitude0
ClinVar
Risk rs199473105(C;C)
Alt rs199473105(C;C)
Reference rs199473105(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.38647590A>G
CLNSRC ClinVar
CLNACC RCV000058401.2,