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rs199473567

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473567(A;A)
Make rs199473567(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38606132
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473567
ebirs199473567
HLIrs199473567
Exacrs199473567
Varsomers199473567
Maprs199473567
PheGenIrs199473567
hapmaprs199473567
1000 genomesrs199473567
hgdprs199473567
ensemblrs199473567
gopubmedrs199473567
geneviewrs199473567
scholarrs199473567
googlers199473567
pharmgkbrs199473567
gwascentralrs199473567
openSNPrs199473567
23andMers199473567
23andMe allrs199473567
SNP Nexus

SNPshotrs199473567
SNPdbers199473567
MSV3drs199473567
GWAS Ctlgrs199473567
Max Magnitude0
ClinVar
Risk rs199473567(A;A)
Alt rs199473567(A;A)
Reference rs199473567(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38647623C>T
CLNSRC ClinVar
CLNACC RCV000058398.2,