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rs199473228

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473228(C;C)
Make rs199473228(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38560362
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473228
ebirs199473228
HLIrs199473228
Exacrs199473228
Varsomers199473228
Maprs199473228
PheGenIrs199473228
hapmaprs199473228
1000 genomesrs199473228
hgdprs199473228
ensemblrs199473228
gopubmedrs199473228
geneviewrs199473228
scholarrs199473228
googlers199473228
pharmgkbrs199473228
gwascentralrs199473228
openSNPrs199473228
23andMers199473228
23andMe allrs199473228
SNP Nexus

SNPshotrs199473228
SNPdbers199473228
MSV3drs199473228
GWAS Ctlgrs199473228
Max Magnitude0
ClinVar
Risk rs199473228(C;C)
Alt rs199473228(C;C)
Reference rs199473228(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38601853A>G
CLNSRC ClinVar
CLNACC RCV000058629.2,