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rs199473063

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473063(C;C)
Make rs199473063(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38620929
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473063
ebirs199473063
HLIrs199473063
Exacrs199473063
Varsomers199473063
Maprs199473063
PheGenIrs199473063
hapmaprs199473063
1000 genomesrs199473063
hgdprs199473063
ensemblrs199473063
gopubmedrs199473063
geneviewrs199473063
scholarrs199473063
googlers199473063
pharmgkbrs199473063
gwascentralrs199473063
openSNPrs199473063
23andMers199473063
23andMe allrs199473063
SNP Nexus

SNPshotrs199473063
SNPdbers199473063
MSV3drs199473063
GWAS Ctlgrs199473063
Max Magnitude0
ClinVar
Risk rs199473063(C;C)
Alt rs199473063(C;C)
Reference rs199473063(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38662420C>G
CLNSRC ClinVar
CLNACC RCV000058757.2,