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rs199473298

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473298(A;A)
Make rs199473298(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551238
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473298
ebirs199473298
HLIrs199473298
Exacrs199473298
Varsomers199473298
Maprs199473298
PheGenIrs199473298
hapmaprs199473298
1000 genomesrs199473298
hgdprs199473298
ensemblrs199473298
gopubmedrs199473298
geneviewrs199473298
scholarrs199473298
googlers199473298
pharmgkbrs199473298
gwascentralrs199473298
openSNPrs199473298
23andMers199473298
23andMe allrs199473298
SNP Nexus

SNPshotrs199473298
SNPdbers199473298
MSV3drs199473298
GWAS Ctlgrs199473298
Max Magnitude0
ClinVar
Risk rs199473298(A;A)
Alt rs199473298(A;A)
Reference rs199473298(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38592729C>T
CLNSRC ClinVar
CLNACC RCV000058744.2,