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rs794728847

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728847(G;T)
Make rs794728847(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38620915
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728847
ebirs794728847
HLIrs794728847
Exacrs794728847
Varsomers794728847
Maprs794728847
PheGenIrs794728847
hapmaprs794728847
1000 genomesrs794728847
hgdprs794728847
ensemblrs794728847
gopubmedrs794728847
geneviewrs794728847
scholarrs794728847
googlers794728847
pharmgkbrs794728847
gwascentralrs794728847
openSNPrs794728847
23andMers794728847
23andMe allrs794728847
SNP Nexus

SNPshotrs794728847
SNPdbers794728847
MSV3drs794728847
GWAS Ctlgrs794728847
Max Magnitude0
ClinVar
Risk rs794728847(T;T)
Alt rs794728847(T;T)
Reference rs794728847(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38662406C>A
CLNSRC
CLNACC RCV000182929.1,