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rs777689378

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs777689378(C;C)
Make rs777689378(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38609884
GeneSCN5A
is asnp
is mentioned by
dbSNPrs777689378
ebirs777689378
HLIrs777689378
Exacrs777689378
Varsomers777689378
Maprs777689378
PheGenIrs777689378
hapmaprs777689378
1000 genomesrs777689378
hgdprs777689378
ensemblrs777689378
gopubmedrs777689378
geneviewrs777689378
scholarrs777689378
googlers777689378
pharmgkbrs777689378
gwascentralrs777689378
openSNPrs777689378
23andMers777689378
23andMe allrs777689378
SNP Nexus

SNPshotrs777689378
SNPdbers777689378
MSV3drs777689378
GWAS Ctlgrs777689378
Max Magnitude0
ClinVar
Risk rs777689378(C,G;C,G)
Alt rs777689378(C,G;C,G)
Reference rs777689378(T;T)
Significance Probable-Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 0
HGVS NC_000003.11:g.38651375T>G
CLNSRC
CLNACC RCV000208042.1,