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rs483353016

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs483353016(A;A)
Make rs483353016(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position38562414
GeneSCN5A
is asnp
is mentioned by
dbSNPrs483353016
ebirs483353016
HLIrs483353016
Exacrs483353016
Varsomers483353016
Maprs483353016
PheGenIrs483353016
hapmaprs483353016
1000 genomesrs483353016
hgdprs483353016
ensemblrs483353016
gopubmedrs483353016
geneviewrs483353016
scholarrs483353016
googlers483353016
pharmgkbrs483353016
gwascentralrs483353016
openSNPrs483353016
23andMers483353016
23andMe allrs483353016
SNP Nexus

SNPshotrs483353016
SNPdbers483353016
MSV3drs483353016
GWAS Ctlgrs483353016
Max Magnitude0
ClinVar
Risk rs483353016(A;A)
Alt rs483353016(A;A)
Reference rs483353016(G;G)
Significance Probable-Pathogenic
Disease not provided Brugada syndrome
Variation info
Gene SCN5A
CLNDBN not provided Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38603905C>T
CLNSRC
CLNACC RCV000149447.1, RCV000155938.1,