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

rs199473096

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473096(C;T)
Make rs199473096(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38606751
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473096
ebirs199473096
HLIrs199473096
Exacrs199473096
Varsomers199473096
Maprs199473096
PheGenIrs199473096
hapmaprs199473096
1000 genomesrs199473096
hgdprs199473096
ensemblrs199473096
gopubmedrs199473096
geneviewrs199473096
scholarrs199473096
googlers199473096
pharmgkbrs199473096
gwascentralrs199473096
openSNPrs199473096
23andMers199473096
23andMe allrs199473096
SNP Nexus

SNPshotrs199473096
SNPdbers199473096
MSV3drs199473096
GWAS Ctlgrs199473096
Max Magnitude0
ClinVar
Risk rs199473096(T;T)
Alt rs199473096(T;T)
Reference rs199473096(C;C)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38648242G>A
CLNSRC ClinVar
CLNACC RCV000058387.2,