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rs794728890

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728890(A;G)
Make rs794728890(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38551346
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728890
ebirs794728890
HLIrs794728890
Exacrs794728890
Varsomers794728890
Maprs794728890
PheGenIrs794728890
hapmaprs794728890
1000 genomesrs794728890
hgdprs794728890
ensemblrs794728890
gopubmedrs794728890
geneviewrs794728890
scholarrs794728890
googlers794728890
pharmgkbrs794728890
gwascentralrs794728890
openSNPrs794728890
23andMers794728890
23andMe allrs794728890
SNP Nexus

SNPshotrs794728890
SNPdbers794728890
MSV3drs794728890
GWAS Ctlgrs794728890
Max Magnitude0
ClinVar
Risk rs794728890(G;G)
Alt rs794728890(G;G)
Reference rs794728890(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38592837T>C
CLNSRC
CLNACC RCV000183096.1,