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rs199473296

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473296(C;C)
Make rs199473296(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551254
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473296
ebirs199473296
HLIrs199473296
Exacrs199473296
Varsomers199473296
Maprs199473296
PheGenIrs199473296
hapmaprs199473296
1000 genomesrs199473296
hgdprs199473296
ensemblrs199473296
gopubmedrs199473296
geneviewrs199473296
scholarrs199473296
googlers199473296
pharmgkbrs199473296
gwascentralrs199473296
openSNPrs199473296
23andMers199473296
23andMe allrs199473296
SNP Nexus

SNPshotrs199473296
SNPdbers199473296
MSV3drs199473296
GWAS Ctlgrs199473296
Max Magnitude0
ClinVar
Risk rs199473296(C;C)
Alt rs199473296(C;C)
Reference rs199473296(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38592745C>G
CLNSRC ClinVar
CLNACC RCV000058740.2,