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rs794728902

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728902(-;-)
Make rs794728902(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38633251
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728902
ebirs794728902
HLIrs794728902
Exacrs794728902
Varsomers794728902
Maprs794728902
PheGenIrs794728902
hapmaprs794728902
1000 genomesrs794728902
hgdprs794728902
ensemblrs794728902
gopubmedrs794728902
geneviewrs794728902
scholarrs794728902
googlers794728902
pharmgkbrs794728902
gwascentralrs794728902
openSNPrs794728902
23andMers794728902
23andMe allrs794728902
SNP Nexus

SNPshotrs794728902
SNPdbers794728902
MSV3drs794728902
GWAS Ctlgrs794728902
Max Magnitude0
ClinVar
Risk rs794728902(;)
Alt rs794728902(;)
Reference rs794728902(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38674742delC
CLNSRC
CLNACC RCV000183138.1,