Have questions? Visit https://www.reddit.com/r/SNPedia

rs199473322

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473322(C;C)
Make rs199473322(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38550823
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473322
ebirs199473322
HLIrs199473322
Exacrs199473322
Varsomers199473322
Maprs199473322
PheGenIrs199473322
hapmaprs199473322
1000 genomesrs199473322
hgdprs199473322
ensemblrs199473322
gopubmedrs199473322
geneviewrs199473322
scholarrs199473322
googlers199473322
pharmgkbrs199473322
gwascentralrs199473322
openSNPrs199473322
23andMers199473322
23andMe allrs199473322
SNP Nexus

SNPshotrs199473322
SNPdbers199473322
MSV3drs199473322
GWAS Ctlgrs199473322
Max Magnitude0
ClinVar
Risk rs199473322(C;C)
Alt rs199473322(C;C)
Reference rs199473322(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38592314C>G
CLNSRC ClinVar
CLNACC RCV000058791.2,