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rs199473079

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473079(A;A)
Make rs199473079(A;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position38609860
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473079
ebirs199473079
HLIrs199473079
Exacrs199473079
Varsomers199473079
Maprs199473079
PheGenIrs199473079
hapmaprs199473079
1000 genomesrs199473079
hgdprs199473079
ensemblrs199473079
gopubmedrs199473079
geneviewrs199473079
scholarrs199473079
googlers199473079
pharmgkbrs199473079
gwascentralrs199473079
openSNPrs199473079
23andMers199473079
23andMe allrs199473079
SNP Nexus

SNPshotrs199473079
SNPdbers199473079
MSV3drs199473079
GWAS Ctlgrs199473079
Max Magnitude0
ClinVar
Risk rs199473079(A;A)
Alt rs199473079(A;A)
Reference rs199473079(C;C)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38651351G>T
CLNSRC ClinVar
CLNACC RCV000058845.2,