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

rs863225273

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225273(A;A)
Make rs863225273(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38554320
GeneSCN5A
is asnp
is mentioned by
dbSNPrs863225273
ebirs863225273
HLIrs863225273
Exacrs863225273
Varsomers863225273
Maprs863225273
PheGenIrs863225273
hapmaprs863225273
1000 genomesrs863225273
hgdprs863225273
ensemblrs863225273
gopubmedrs863225273
geneviewrs863225273
scholarrs863225273
googlers863225273
pharmgkbrs863225273
gwascentralrs863225273
openSNPrs863225273
23andMers863225273
23andMe allrs863225273
SNP Nexus

SNPshotrs863225273
SNPdbers863225273
MSV3drs863225273
GWAS Ctlgrs863225273
Max Magnitude0
ClinVar
Risk rs863225273(A;A)
Alt rs863225273(A;A)
Reference rs863225273(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38595811C>T
CLNSRC
CLNACC RCV000201896.1,