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rs794728939

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728939(A;A)
Make rs794728939(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38550764
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728939
ebirs794728939
HLIrs794728939
Exacrs794728939
Varsomers794728939
Maprs794728939
PheGenIrs794728939
hapmaprs794728939
1000 genomesrs794728939
hgdprs794728939
ensemblrs794728939
gopubmedrs794728939
geneviewrs794728939
scholarrs794728939
googlers794728939
pharmgkbrs794728939
gwascentralrs794728939
openSNPrs794728939
23andMers794728939
23andMe allrs794728939
SNP Nexus

SNPshotrs794728939
SNPdbers794728939
MSV3drs794728939
GWAS Ctlgrs794728939
Max Magnitude0
ClinVar
Risk rs794728939(A;A)
Alt rs794728939(A;A)
Reference rs794728939(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38592255C>T
CLNSRC
CLNACC RCV000183201.1,