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rs199473251

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473251(C;C)
Make rs199473251(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38556535
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473251
ebirs199473251
HLIrs199473251
Exacrs199473251
Varsomers199473251
Maprs199473251
PheGenIrs199473251
hapmaprs199473251
1000 genomesrs199473251
hgdprs199473251
ensemblrs199473251
gopubmedrs199473251
geneviewrs199473251
scholarrs199473251
googlers199473251
pharmgkbrs199473251
gwascentralrs199473251
openSNPrs199473251
23andMers199473251
23andMe allrs199473251
SNP Nexus

SNPshotrs199473251
SNPdbers199473251
MSV3drs199473251
GWAS Ctlgrs199473251
Max Magnitude0
ClinVar
Risk rs199473251(C;C)
Alt rs199473251(C;C)
Reference rs199473251(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38598026A>G
CLNSRC ClinVar
CLNACC RCV000058663.2,