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rs199473149

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473149(C;T)
Make rs199473149(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38597841
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473149
ebirs199473149
HLIrs199473149
Exacrs199473149
Varsomers199473149
Maprs199473149
PheGenIrs199473149
hapmaprs199473149
1000 genomesrs199473149
hgdprs199473149
ensemblrs199473149
gopubmedrs199473149
geneviewrs199473149
scholarrs199473149
googlers199473149
pharmgkbrs199473149
gwascentralrs199473149
openSNPrs199473149
23andMers199473149
23andMe allrs199473149
SNP Nexus

SNPshotrs199473149
SNPdbers199473149
MSV3drs199473149
GWAS Ctlgrs199473149
Max Magnitude0
ClinVar
Risk rs199473149(T;T)
Alt rs199473149(T;T)
Reference rs199473149(C;C)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38639332G>A
CLNSRC ClinVar
CLNACC RCV000058484.2,