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rs199473587

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473587(A;A)
Make rs199473587(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38585845
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473587
ebirs199473587
HLIrs199473587
Exacrs199473587
Varsomers199473587
Maprs199473587
PheGenIrs199473587
hapmaprs199473587
1000 genomesrs199473587
hgdprs199473587
ensemblrs199473587
gopubmedrs199473587
geneviewrs199473587
scholarrs199473587
googlers199473587
pharmgkbrs199473587
gwascentralrs199473587
openSNPrs199473587
23andMers199473587
23andMe allrs199473587
SNP Nexus

SNPshotrs199473587
SNPdbers199473587
MSV3drs199473587
GWAS Ctlgrs199473587
Max Magnitude0
ClinVar
Risk rs199473587(A;A)
Alt rs199473587(A;A)
Reference rs199473587(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38627336C>T
CLNSRC ClinVar
CLNACC RCV000058514.2,