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rs199473238

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473238(C;G)
Make rs199473238(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38560252
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473238
ebirs199473238
HLIrs199473238
Exacrs199473238
Varsomers199473238
Maprs199473238
PheGenIrs199473238
hapmaprs199473238
1000 genomesrs199473238
hgdprs199473238
ensemblrs199473238
gopubmedrs199473238
geneviewrs199473238
scholarrs199473238
googlers199473238
pharmgkbrs199473238
gwascentralrs199473238
openSNPrs199473238
23andMers199473238
23andMe allrs199473238
SNP Nexus

SNPshotrs199473238
SNPdbers199473238
MSV3drs199473238
GWAS Ctlgrs199473238
Max Magnitude0
ClinVar
Risk rs199473238(G;G)
Alt rs199473238(G;G)
Reference rs199473238(C;C)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38601743G>C
CLNSRC ClinVar
CLNACC RCV000058642.2,