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rs794728938

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728938(C;C)
Make rs794728938(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38554279
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728938
ebirs794728938
HLIrs794728938
Exacrs794728938
Varsomers794728938
Maprs794728938
PheGenIrs794728938
hapmaprs794728938
1000 genomesrs794728938
hgdprs794728938
ensemblrs794728938
gopubmedrs794728938
geneviewrs794728938
scholarrs794728938
googlers794728938
pharmgkbrs794728938
gwascentralrs794728938
openSNPrs794728938
23andMers794728938
23andMe allrs794728938
SNP Nexus

SNPshotrs794728938
SNPdbers794728938
MSV3drs794728938
GWAS Ctlgrs794728938
Max Magnitude0
ClinVar
Risk rs794728938(C;C)
Alt rs794728938(C;C)
Reference rs794728938(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38595770C>G
CLNSRC
CLNACC RCV000183197.1,