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rs199473109

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473109(C;G)
Make rs199473109(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38606064
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473109
ebirs199473109
HLIrs199473109
Exacrs199473109
Varsomers199473109
Maprs199473109
PheGenIrs199473109
hapmaprs199473109
1000 genomesrs199473109
hgdprs199473109
ensemblrs199473109
gopubmedrs199473109
geneviewrs199473109
scholarrs199473109
googlers199473109
pharmgkbrs199473109
gwascentralrs199473109
openSNPrs199473109
23andMers199473109
23andMe allrs199473109
SNP Nexus

SNPshotrs199473109
SNPdbers199473109
MSV3drs199473109
GWAS Ctlgrs199473109
Max Magnitude0
ClinVar
Risk rs199473109(G;G)
Alt rs199473109(G;G)
Reference rs199473109(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.38647555G>C
CLNSRC ClinVar
CLNACC RCV000058407.2,