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rs199473597

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473597(A;A)
Make rs199473597(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38575307
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473597
ebirs199473597
HLIrs199473597
Exacrs199473597
Varsomers199473597
Maprs199473597
PheGenIrs199473597
hapmaprs199473597
1000 genomesrs199473597
hgdprs199473597
ensemblrs199473597
gopubmedrs199473597
geneviewrs199473597
scholarrs199473597
googlers199473597
pharmgkbrs199473597
gwascentralrs199473597
openSNPrs199473597
23andMers199473597
23andMe allrs199473597
SNP Nexus

SNPshotrs199473597
SNPdbers199473597
MSV3drs199473597
GWAS Ctlgrs199473597
Max Magnitude0
ClinVar
Risk rs199473597(A;A)
Alt rs199473597(A;A)
Reference rs199473597(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38616798C>T
CLNSRC ClinVar
CLNACC RCV000058584.2,