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rs199473313

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473313(A;G)
Make rs199473313(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551051
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473313
ebirs199473313
HLIrs199473313
Exacrs199473313
Varsomers199473313
Maprs199473313
PheGenIrs199473313
hapmaprs199473313
1000 genomesrs199473313
hgdprs199473313
ensemblrs199473313
gopubmedrs199473313
geneviewrs199473313
scholarrs199473313
googlers199473313
pharmgkbrs199473313
gwascentralrs199473313
openSNPrs199473313
23andMers199473313
23andMe allrs199473313
SNP Nexus

SNPshotrs199473313
SNPdbers199473313
MSV3drs199473313
GWAS Ctlgrs199473313
Max Magnitude0
ClinVar
Risk rs199473313(G;G)
Alt rs199473313(G;G)
Reference rs199473313(A;A)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38592542T>C
CLNSRC ClinVar
CLNACC RCV000058769.2,