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

rs199473289

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473289(C;T)
Make rs199473289(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551426
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473289
ebirs199473289
HLIrs199473289
Exacrs199473289
Varsomers199473289
Maprs199473289
PheGenIrs199473289
hapmaprs199473289
1000 genomesrs199473289
hgdprs199473289
ensemblrs199473289
gopubmedrs199473289
geneviewrs199473289
scholarrs199473289
googlers199473289
pharmgkbrs199473289
gwascentralrs199473289
openSNPrs199473289
23andMers199473289
23andMe allrs199473289
SNP Nexus

SNPshotrs199473289
SNPdbers199473289
MSV3drs199473289
GWAS Ctlgrs199473289
Max Magnitude0
ClinVar
Risk rs199473289(T;T)
Alt rs199473289(T;T)
Reference rs199473289(C;C)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38592917G>A
CLNSRC ClinVar
CLNACC RCV000058728.2,