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rs199473093

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473093(C;T)
Make rs199473093(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38606802
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473093
ebirs199473093
HLIrs199473093
Exacrs199473093
Varsomers199473093
Maprs199473093
PheGenIrs199473093
hapmaprs199473093
1000 genomesrs199473093
hgdprs199473093
ensemblrs199473093
gopubmedrs199473093
geneviewrs199473093
scholarrs199473093
googlers199473093
pharmgkbrs199473093
gwascentralrs199473093
openSNPrs199473093
23andMers199473093
23andMe allrs199473093
SNP Nexus

SNPshotrs199473093
SNPdbers199473093
MSV3drs199473093
GWAS Ctlgrs199473093
Max Magnitude0
ClinVar
Risk rs199473093(T;T)
Alt rs199473093(T;T)
Reference rs199473093(C;C)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38648293G>A
CLNSRC ClinVar
CLNACC RCV000058379.2,