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

rs199473183

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473183(C;C)
Make rs199473183(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38581149
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473183
ebirs199473183
HLIrs199473183
Exacrs199473183
Varsomers199473183
Maprs199473183
PheGenIrs199473183
hapmaprs199473183
1000 genomesrs199473183
hgdprs199473183
ensemblrs199473183
gopubmedrs199473183
geneviewrs199473183
scholarrs199473183
googlers199473183
pharmgkbrs199473183
gwascentralrs199473183
openSNPrs199473183
23andMers199473183
23andMe allrs199473183
SNP Nexus

SNPshotrs199473183
SNPdbers199473183
MSV3drs199473183
GWAS Ctlgrs199473183
Max Magnitude0
ClinVar
Risk rs199473183(C;C)
Alt rs199473183(C;C)
Reference rs199473183(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome not specified
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome not specified
Reversed 1
HGVS NC_000003.11:g.38622640A>G
CLNSRC ClinVar
CLNACC RCV000058543.2, RCV000155885.1,