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rs794728891

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728891(C;C)
Make rs794728891(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38551300
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728891
ebirs794728891
HLIrs794728891
Exacrs794728891
Varsomers794728891
Maprs794728891
PheGenIrs794728891
hapmaprs794728891
1000 genomesrs794728891
hgdprs794728891
ensemblrs794728891
gopubmedrs794728891
geneviewrs794728891
scholarrs794728891
googlers794728891
pharmgkbrs794728891
gwascentralrs794728891
openSNPrs794728891
23andMers794728891
23andMe allrs794728891
SNP Nexus

SNPshotrs794728891
SNPdbers794728891
MSV3drs794728891
GWAS Ctlgrs794728891
Max Magnitude0
ClinVar
Risk rs794728891(C;C)
Alt rs794728891(C;C)
Reference rs794728891(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38592791A>G
CLNSRC
CLNACC RCV000183099.2,