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rs794728935

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728935(C;C)
Make rs794728935(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38557231
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728935
ebirs794728935
HLIrs794728935
Exacrs794728935
Varsomers794728935
Maprs794728935
PheGenIrs794728935
hapmaprs794728935
1000 genomesrs794728935
hgdprs794728935
ensemblrs794728935
gopubmedrs794728935
geneviewrs794728935
scholarrs794728935
googlers794728935
pharmgkbrs794728935
gwascentralrs794728935
openSNPrs794728935
23andMers794728935
23andMe allrs794728935
SNP Nexus

SNPshotrs794728935
SNPdbers794728935
MSV3drs794728935
GWAS Ctlgrs794728935
Max Magnitude0
ClinVar
Risk rs794728935(C;C)
Alt rs794728935(C;C)
Reference rs794728935(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38598722C>G
CLNSRC
CLNACC RCV000183191.1,