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rs199473274

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473274(G;G)
Make rs199473274(G;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38554380
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473274
ebirs199473274
HLIrs199473274
Exacrs199473274
Varsomers199473274
Maprs199473274
PheGenIrs199473274
hapmaprs199473274
1000 genomesrs199473274
hgdprs199473274
ensemblrs199473274
gopubmedrs199473274
geneviewrs199473274
scholarrs199473274
googlers199473274
pharmgkbrs199473274
gwascentralrs199473274
openSNPrs199473274
23andMers199473274
23andMe allrs199473274
SNP Nexus

SNPshotrs199473274
SNPdbers199473274
MSV3drs199473274
GWAS Ctlgrs199473274
Max Magnitude0
ClinVar
Risk rs199473274(G;G)
Alt rs199473274(G;G)
Reference rs199473274(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38595871A>C
CLNSRC ClinVar
CLNACC RCV000058698.2,