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rs199473098

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473098(A;A)
Make rs199473098(A;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38606703
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473098
ebirs199473098
HLIrs199473098
Exacrs199473098
Varsomers199473098
Maprs199473098
PheGenIrs199473098
hapmaprs199473098
1000 genomesrs199473098
hgdprs199473098
ensemblrs199473098
gopubmedrs199473098
geneviewrs199473098
scholarrs199473098
googlers199473098
pharmgkbrs199473098
gwascentralrs199473098
openSNPrs199473098
23andMers199473098
23andMe allrs199473098
SNP Nexus

SNPshotrs199473098
SNPdbers199473098
MSV3drs199473098
GWAS Ctlgrs199473098
Max Magnitude0
ClinVar
Risk rs199473098(A;A)
Alt rs199473098(A;A)
Reference rs199473098(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38648194A>T
CLNSRC ClinVar
CLNACC RCV000058392.2,