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rs794728893

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728893(A;A)
Make rs794728893(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38551232
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728893
ebirs794728893
HLIrs794728893
Exacrs794728893
Varsomers794728893
Maprs794728893
PheGenIrs794728893
hapmaprs794728893
1000 genomesrs794728893
hgdprs794728893
ensemblrs794728893
gopubmedrs794728893
geneviewrs794728893
scholarrs794728893
googlers794728893
pharmgkbrs794728893
gwascentralrs794728893
openSNPrs794728893
23andMers794728893
23andMe allrs794728893
SNP Nexus

SNPshotrs794728893
SNPdbers794728893
MSV3drs794728893
GWAS Ctlgrs794728893
Max Magnitude0
ClinVar
Risk rs794728893(A;A)
Alt rs794728893(A;A)
Reference rs794728893(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38592723C>T
CLNSRC
CLNACC RCV000183103.1,