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rs794728886

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728886(A;G)
Make rs794728886(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38555745
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728886
ebirs794728886
HLIrs794728886
Exacrs794728886
Varsomers794728886
Maprs794728886
PheGenIrs794728886
hapmaprs794728886
1000 genomesrs794728886
hgdprs794728886
ensemblrs794728886
gopubmedrs794728886
geneviewrs794728886
scholarrs794728886
googlers794728886
pharmgkbrs794728886
gwascentralrs794728886
openSNPrs794728886
23andMers794728886
23andMe allrs794728886
SNP Nexus

SNPshotrs794728886
SNPdbers794728886
MSV3drs794728886
GWAS Ctlgrs794728886
Max Magnitude0
ClinVar
Risk rs794728886(G;G)
Alt rs794728886(G;G)
Reference rs794728886(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38597236T>C
CLNSRC
CLNACC RCV000183077.1,