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rs199473231

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473231(C;C)
Make rs199473231(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38560355
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473231
ebirs199473231
HLIrs199473231
Exacrs199473231
Varsomers199473231
Maprs199473231
PheGenIrs199473231
hapmaprs199473231
1000 genomesrs199473231
hgdprs199473231
ensemblrs199473231
gopubmedrs199473231
geneviewrs199473231
scholarrs199473231
googlers199473231
pharmgkbrs199473231
gwascentralrs199473231
openSNPrs199473231
23andMers199473231
23andMe allrs199473231
SNP Nexus

SNPshotrs199473231
SNPdbers199473231
MSV3drs199473231
GWAS Ctlgrs199473231
Max Magnitude0
ClinVar
Risk rs199473231(C;C)
Alt rs199473231(C;C)
Reference rs199473231(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38601846A>G
CLNSRC ClinVar
CLNACC RCV000058633.2,