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rs199473137

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473137(C;G)
Make rs199473137(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38599023
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473137
ebirs199473137
HLIrs199473137
Exacrs199473137
Varsomers199473137
Maprs199473137
PheGenIrs199473137
hapmaprs199473137
1000 genomesrs199473137
hgdprs199473137
ensemblrs199473137
gopubmedrs199473137
geneviewrs199473137
scholarrs199473137
googlers199473137
pharmgkbrs199473137
gwascentralrs199473137
openSNPrs199473137
23andMers199473137
23andMe allrs199473137
SNP Nexus

SNPshotrs199473137
SNPdbers199473137
MSV3drs199473137
GWAS Ctlgrs199473137
Max Magnitude0
ClinVar
Risk rs199473137(G,T;G,T)
Alt rs199473137(G,T;G,T)
Reference rs199473137(C;C)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38640514G>C
CLNSRC ClinVar
CLNACC RCV000058464.2,