Have questions? Visit https://www.reddit.com/r/SNPedia

rs199473583

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473583(A;A)
Make rs199473583(A;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position38587501
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473583
ebirs199473583
HLIrs199473583
Exacrs199473583
Varsomers199473583
Maprs199473583
PheGenIrs199473583
hapmaprs199473583
1000 genomesrs199473583
hgdprs199473583
ensemblrs199473583
gopubmedrs199473583
geneviewrs199473583
scholarrs199473583
googlers199473583
pharmgkbrs199473583
gwascentralrs199473583
openSNPrs199473583
23andMers199473583
23andMe allrs199473583
SNP Nexus

SNPshotrs199473583
SNPdbers199473583
MSV3drs199473583
GWAS Ctlgrs199473583
Max Magnitude0
ClinVar
Risk rs199473583(A;A)
Alt rs199473583(A;A)
Reference rs199473583(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.38628992G>T
CLNSRC ClinVar
CLNACC RCV000058497.2,