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

rs199473303

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473303(C;T)
Make rs199473303(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551157
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473303
ebirs199473303
HLIrs199473303
Exacrs199473303
Varsomers199473303
Maprs199473303
PheGenIrs199473303
hapmaprs199473303
1000 genomesrs199473303
hgdprs199473303
ensemblrs199473303
gopubmedrs199473303
geneviewrs199473303
scholarrs199473303
googlers199473303
pharmgkbrs199473303
gwascentralrs199473303
openSNPrs199473303
23andMers199473303
23andMe allrs199473303
SNP Nexus

SNPshotrs199473303
SNPdbers199473303
MSV3drs199473303
GWAS Ctlgrs199473303
Max Magnitude0
ClinVar
Risk rs199473303(A,T;A,T)
Alt rs199473303(A,T;A,T)
Reference rs199473303(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.38592648G>A
CLNSRC ClinVar
CLNACC RCV000058751.2,