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rs199473588

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473588(C;C)
Make rs199473588(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38585735
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473588
ebirs199473588
HLIrs199473588
Exacrs199473588
Varsomers199473588
Maprs199473588
PheGenIrs199473588
hapmaprs199473588
1000 genomesrs199473588
hgdprs199473588
ensemblrs199473588
gopubmedrs199473588
geneviewrs199473588
scholarrs199473588
googlers199473588
pharmgkbrs199473588
gwascentralrs199473588
openSNPrs199473588
23andMers199473588
23andMe allrs199473588
SNP Nexus

SNPshotrs199473588
SNPdbers199473588
MSV3drs199473588
GWAS Ctlgrs199473588
Max Magnitude0
ClinVar
Risk rs199473588(C;C)
Alt rs199473588(C;C)
Reference rs199473588(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38627226A>G
CLNSRC ClinVar
CLNACC RCV000058523.2,