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rs863224533

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
Make rs863224533(CTT;GTA)
Make rs863224533(GTA;GTA)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38551525
GeneSCN5A
is asnp
is mentioned by
dbSNPrs863224533
ClinGenrs863224533
ebirs863224533
HLIrs863224533
Exacrs863224533
Varsomers863224533
Maprs863224533
PheGenIrs863224533
hapmaprs863224533
1000 genomesrs863224533
hgdprs863224533
ensemblrs863224533
gopubmedrs863224533
geneviewrs863224533
scholarrs863224533
googlers863224533
pharmgkbrs863224533
gwascentralrs863224533
openSNPrs863224533
23andMers863224533
23andMe allrs863224533
SNP Nexus

SNPshotrs863224533
SNPdbers863224533
MSV3drs863224533
GWAS Ctlgrs863224533
Max Magnitude0
ClinVar
Risk rs863224533(GTA;GTA)
Alt rs863224533(GTA;GTA)
Reference Rs863224533(CTT;CTT)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38593016_38593018delAAGinsTAC
CLNSRC
CLNACC RCV000195716.1,