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rs199473314

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473314(A;A)
Make rs199473314(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551043
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473314
ebirs199473314
HLIrs199473314
Exacrs199473314
Varsomers199473314
Maprs199473314
PheGenIrs199473314
hapmaprs199473314
1000 genomesrs199473314
hgdprs199473314
ensemblrs199473314
gopubmedrs199473314
geneviewrs199473314
scholarrs199473314
googlers199473314
pharmgkbrs199473314
gwascentralrs199473314
openSNPrs199473314
23andMers199473314
23andMe allrs199473314
SNP Nexus

SNPshotrs199473314
SNPdbers199473314
MSV3drs199473314
GWAS Ctlgrs199473314
Max Magnitude0
ClinVar
Risk rs199473314(A;A)
Alt rs199473314(A;A)
Reference rs199473314(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome not provided
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38592534C>T
CLNSRC ClinVar
CLNACC RCV000058770.2, RCV000183114.2,