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rs794728889

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728889(A;G)
Make rs794728889(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38551421
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728889
ebirs794728889
HLIrs794728889
Exacrs794728889
Varsomers794728889
Maprs794728889
PheGenIrs794728889
hapmaprs794728889
1000 genomesrs794728889
hgdprs794728889
ensemblrs794728889
gopubmedrs794728889
geneviewrs794728889
scholarrs794728889
googlers794728889
pharmgkbrs794728889
gwascentralrs794728889
openSNPrs794728889
23andMers794728889
23andMe allrs794728889
SNP Nexus

SNPshotrs794728889
SNPdbers794728889
MSV3drs794728889
GWAS Ctlgrs794728889
Max Magnitude0
ClinVar
Risk rs794728889(G;G)
Alt rs794728889(G;G)
Reference rs794728889(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38592912T>C
CLNSRC
CLNACC RCV000183092.2,