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rs863224532

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224532(C;G)
Make rs863224532(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38560210
GeneSCN5A
is asnp
is mentioned by
dbSNPrs863224532
ebirs863224532
HLIrs863224532
Exacrs863224532
Varsomers863224532
Maprs863224532
PheGenIrs863224532
hapmaprs863224532
1000 genomesrs863224532
hgdprs863224532
ensemblrs863224532
gopubmedrs863224532
geneviewrs863224532
scholarrs863224532
googlers863224532
pharmgkbrs863224532
gwascentralrs863224532
openSNPrs863224532
23andMers863224532
23andMe allrs863224532
SNP Nexus

SNPshotrs863224532
SNPdbers863224532
MSV3drs863224532
GWAS Ctlgrs863224532
Max Magnitude0
ClinVar
Risk rs863224532(G;G)
Alt rs863224532(G;G)
Reference rs863224532(C;C)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38601701G>C
CLNSRC
CLNACC RCV000199303.1,