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rs199473249

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473249(C;C)
Make rs199473249(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38556557
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473249
ebirs199473249
HLIrs199473249
Exacrs199473249
Varsomers199473249
Maprs199473249
PheGenIrs199473249
hapmaprs199473249
1000 genomesrs199473249
hgdprs199473249
ensemblrs199473249
gopubmedrs199473249
geneviewrs199473249
scholarrs199473249
googlers199473249
pharmgkbrs199473249
gwascentralrs199473249
openSNPrs199473249
23andMers199473249
23andMe allrs199473249
SNP Nexus

SNPshotrs199473249
SNPdbers199473249
MSV3drs199473249
GWAS Ctlgrs199473249
Max Magnitude0
ClinVar
Risk rs199473249(C;C)
Alt rs199473249(C;C)
Reference rs199473249(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38598048C>G
CLNSRC ClinVar
CLNACC RCV000058661.2,