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rs794728859

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728859(A;G)
Make rs794728859(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38581373
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728859
ebirs794728859
HLIrs794728859
Exacrs794728859
Varsomers794728859
Maprs794728859
PheGenIrs794728859
hapmaprs794728859
1000 genomesrs794728859
hgdprs794728859
ensemblrs794728859
gopubmedrs794728859
geneviewrs794728859
scholarrs794728859
googlers794728859
pharmgkbrs794728859
gwascentralrs794728859
openSNPrs794728859
23andMers794728859
23andMe allrs794728859
SNP Nexus

SNPshotrs794728859
SNPdbers794728859
MSV3drs794728859
GWAS Ctlgrs794728859
Max Magnitude0
ClinVar
Risk rs794728859(G;G)
Alt rs794728859(G;G)
Reference rs794728859(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38622864T>C
CLNSRC
CLNACC RCV000182990.1,