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

rs794728914

From SNPedia

Orientationminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs794728914(-;-)
Make rs794728914(-;TT)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38585895
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728914
ebirs794728914
HLIrs794728914
Exacrs794728914
Varsomers794728914
Maprs794728914
PheGenIrs794728914
hapmaprs794728914
1000 genomesrs794728914
hgdprs794728914
ensemblrs794728914
gopubmedrs794728914
geneviewrs794728914
scholarrs794728914
googlers794728914
pharmgkbrs794728914
gwascentralrs794728914
openSNPrs794728914
23andMers794728914
23andMe allrs794728914
SNP Nexus

SNPshotrs794728914
SNPdbers794728914
MSV3drs794728914
GWAS Ctlgrs794728914
Max Magnitude0
ClinVar
Risk rs794728914(;)
Alt rs794728914(;)
Reference rs794728914(TT;TT)
Significance Pathogenic
Disease not provided Brugada syndrome
Variation info
Gene SCN5A
CLNDBN not provided Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38627386_38627387delAA
CLNSRC
CLNACC RCV000183155.1, RCV000201886.1,