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rs794728864

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728864(C;T)
Make rs794728864(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38587405
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728864
ebirs794728864
HLIrs794728864
Exacrs794728864
Varsomers794728864
Maprs794728864
PheGenIrs794728864
hapmaprs794728864
1000 genomesrs794728864
hgdprs794728864
ensemblrs794728864
gopubmedrs794728864
geneviewrs794728864
scholarrs794728864
googlers794728864
pharmgkbrs794728864
gwascentralrs794728864
openSNPrs794728864
23andMers794728864
23andMe allrs794728864
SNP Nexus

SNPshotrs794728864
SNPdbers794728864
MSV3drs794728864
GWAS Ctlgrs794728864
Max Magnitude0
ClinVar
Risk rs794728864(T;T)
Alt rs794728864(T;T)
Reference rs794728864(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38628896G>A
CLNSRC
CLNACC RCV000183002.1,