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rs768579561

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768579561(C;T)
Make rs768579561(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38562414
GeneSCN5A
is asnp
is mentioned by
dbSNPrs768579561
ebirs768579561
HLIrs768579561
Exacrs768579561
Varsomers768579561
Maprs768579561
PheGenIrs768579561
hapmaprs768579561
1000 genomesrs768579561
hgdprs768579561
ensemblrs768579561
gopubmedrs768579561
geneviewrs768579561
scholarrs768579561
googlers768579561
pharmgkbrs768579561
gwascentralrs768579561
openSNPrs768579561
23andMers768579561
23andMe allrs768579561
SNP Nexus

SNPshotrs768579561
SNPdbers768579561
MSV3drs768579561
GWAS Ctlgrs768579561
Max Magnitude0
ClinVar
Risk rs768579561(T;T)
Alt rs768579561(T;T)
Reference rs768579561(C;C)
Significance Probable-Pathogenic
Disease not provided Brugada syndrome 1
Variation info
Gene SCN5A
CLNDBN not provided Brugada syndrome 1
Reversed 0
HGVS NC_000003.11:g.38603905C>T
CLNSRC
CLNACC RCV000149447.1, RCV000155938.1,