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rs199473267

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473267(A;A)
Make rs199473267(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38555694
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473267
ebirs199473267
HLIrs199473267
Exacrs199473267
Varsomers199473267
Maprs199473267
PheGenIrs199473267
hapmaprs199473267
1000 genomesrs199473267
hgdprs199473267
ensemblrs199473267
gopubmedrs199473267
geneviewrs199473267
scholarrs199473267
googlers199473267
pharmgkbrs199473267
gwascentralrs199473267
openSNPrs199473267
23andMers199473267
23andMe allrs199473267
SNP Nexus

SNPshotrs199473267
SNPdbers199473267
MSV3drs199473267
GWAS Ctlgrs199473267
Max Magnitude0
ClinVar
Risk rs199473267(A;A)
Alt rs199473267(A;A)
Reference rs199473267(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38597185C>T
CLNSRC ClinVar
CLNACC RCV000058685.2,