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rs794728851

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728851(A;A)
Make rs794728851(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38606729
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728851
ebirs794728851
HLIrs794728851
Exacrs794728851
Varsomers794728851
Maprs794728851
PheGenIrs794728851
hapmaprs794728851
1000 genomesrs794728851
hgdprs794728851
ensemblrs794728851
gopubmedrs794728851
geneviewrs794728851
scholarrs794728851
googlers794728851
pharmgkbrs794728851
gwascentralrs794728851
openSNPrs794728851
23andMers794728851
23andMe allrs794728851
SNP Nexus

SNPshotrs794728851
SNPdbers794728851
MSV3drs794728851
GWAS Ctlgrs794728851
Max Magnitude0
ClinVar
Risk rs794728851(A;A)
Alt rs794728851(A;A)
Reference rs794728851(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38648220C>T
CLNSRC
CLNACC RCV000182945.1,