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rs199473323

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473323(C;C)
Make rs199473323(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38550756
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473323
ebirs199473323
HLIrs199473323
Exacrs199473323
Varsomers199473323
Maprs199473323
PheGenIrs199473323
hapmaprs199473323
1000 genomesrs199473323
hgdprs199473323
ensemblrs199473323
gopubmedrs199473323
geneviewrs199473323
scholarrs199473323
googlers199473323
pharmgkbrs199473323
gwascentralrs199473323
openSNPrs199473323
23andMers199473323
23andMe allrs199473323
SNP Nexus

SNPshotrs199473323
SNPdbers199473323
MSV3drs199473323
GWAS Ctlgrs199473323
Max Magnitude0
ClinVar
Risk rs199473323(C;C)
Alt rs199473323(C;C)
Reference rs199473323(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38592247C>G
CLNSRC ClinVar
CLNACC RCV000058795.2,