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rs199473589

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473589(A;G)
Make rs199473589(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38585698
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473589
ebirs199473589
HLIrs199473589
Exacrs199473589
Varsomers199473589
Maprs199473589
PheGenIrs199473589
hapmaprs199473589
1000 genomesrs199473589
hgdprs199473589
ensemblrs199473589
gopubmedrs199473589
geneviewrs199473589
scholarrs199473589
googlers199473589
pharmgkbrs199473589
gwascentralrs199473589
openSNPrs199473589
23andMers199473589
23andMe allrs199473589
SNP Nexus

SNPshotrs199473589
SNPdbers199473589
MSV3drs199473589
GWAS Ctlgrs199473589
Max Magnitude0
ClinVar
Risk rs199473589(G;G)
Alt rs199473589(G;G)
Reference rs199473589(A;A)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38627189T>C
CLNSRC ClinVar
CLNACC RCV000058526.2,