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

rs199473089

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473089(C;C)
Make rs199473089(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38608198
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473089
ebirs199473089
HLIrs199473089
Exacrs199473089
Varsomers199473089
Maprs199473089
PheGenIrs199473089
hapmaprs199473089
1000 genomesrs199473089
hgdprs199473089
ensemblrs199473089
gopubmedrs199473089
geneviewrs199473089
scholarrs199473089
googlers199473089
pharmgkbrs199473089
gwascentralrs199473089
openSNPrs199473089
23andMers199473089
23andMe allrs199473089
SNP Nexus

SNPshotrs199473089
SNPdbers199473089
MSV3drs199473089
GWAS Ctlgrs199473089
Max Magnitude0
ClinVar
Risk rs199473089(C;C)
Alt rs199473089(C;C)
Reference rs199473089(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38649689C>G
CLNSRC ClinVar
CLNACC RCV000058863.2,