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rs199473557

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473557(C;C)
Make rs199473557(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38622475
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473557
ebirs199473557
HLIrs199473557
Exacrs199473557
Varsomers199473557
Maprs199473557
PheGenIrs199473557
hapmaprs199473557
1000 genomesrs199473557
hgdprs199473557
ensemblrs199473557
gopubmedrs199473557
geneviewrs199473557
scholarrs199473557
googlers199473557
pharmgkbrs199473557
gwascentralrs199473557
openSNPrs199473557
23andMers199473557
23andMe allrs199473557
SNP Nexus

SNPshotrs199473557
SNPdbers199473557
MSV3drs199473557
GWAS Ctlgrs199473557
Max Magnitude0
ClinVar
Risk rs199473557(C;C)
Alt rs199473557(C;C)
Reference rs199473557(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38663966A>G
CLNSRC ClinVar
CLNACC RCV000058640.2,