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rs199473299

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473299(A;G)
Make rs199473299(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551208
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473299
ebirs199473299
HLIrs199473299
Exacrs199473299
Varsomers199473299
Maprs199473299
PheGenIrs199473299
hapmaprs199473299
1000 genomesrs199473299
hgdprs199473299
ensemblrs199473299
gopubmedrs199473299
geneviewrs199473299
scholarrs199473299
googlers199473299
pharmgkbrs199473299
gwascentralrs199473299
openSNPrs199473299
23andMers199473299
23andMe allrs199473299
SNP Nexus

SNPshotrs199473299
SNPdbers199473299
MSV3drs199473299
GWAS Ctlgrs199473299
Max Magnitude0
ClinVar
Risk rs199473299(G;G)
Alt rs199473299(G;G)
Reference rs199473299(A;A)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38592699T>C
CLNSRC ClinVar
CLNACC RCV000058746.2,