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rs794728848

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728848(G;T)
Make rs794728848(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38620865
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728848
ebirs794728848
HLIrs794728848
Exacrs794728848
Varsomers794728848
Maprs794728848
PheGenIrs794728848
hapmaprs794728848
1000 genomesrs794728848
hgdprs794728848
ensemblrs794728848
gopubmedrs794728848
geneviewrs794728848
scholarrs794728848
googlers794728848
pharmgkbrs794728848
gwascentralrs794728848
openSNPrs794728848
23andMers794728848
23andMe allrs794728848
SNP Nexus

SNPshotrs794728848
SNPdbers794728848
MSV3drs794728848
GWAS Ctlgrs794728848
Max Magnitude0
ClinVar
Risk rs794728848(T;T)
Alt rs794728848(T;T)
Reference rs794728848(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38662356C>A
CLNSRC
CLNACC RCV000182934.1,