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

rs199473273

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473273(C;C)
Make rs199473273(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38554387
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473273
ebirs199473273
HLIrs199473273
Exacrs199473273
Varsomers199473273
Maprs199473273
PheGenIrs199473273
hapmaprs199473273
1000 genomesrs199473273
hgdprs199473273
ensemblrs199473273
gopubmedrs199473273
geneviewrs199473273
scholarrs199473273
googlers199473273
pharmgkbrs199473273
gwascentralrs199473273
openSNPrs199473273
23andMers199473273
23andMe allrs199473273
SNP Nexus

SNPshotrs199473273
SNPdbers199473273
MSV3drs199473273
GWAS Ctlgrs199473273
Max Magnitude0
ClinVar
Risk rs199473273(C;C)
Alt rs199473273(C;C)
Reference rs199473273(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38595878C>G
CLNSRC ClinVar
CLNACC RCV000058697.2,