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rs794728892

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728892(A;A)
Make rs794728892(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38551264
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728892
ebirs794728892
HLIrs794728892
Exacrs794728892
Varsomers794728892
Maprs794728892
PheGenIrs794728892
hapmaprs794728892
1000 genomesrs794728892
hgdprs794728892
ensemblrs794728892
gopubmedrs794728892
geneviewrs794728892
scholarrs794728892
googlers794728892
pharmgkbrs794728892
gwascentralrs794728892
openSNPrs794728892
23andMers794728892
23andMe allrs794728892
SNP Nexus

SNPshotrs794728892
SNPdbers794728892
MSV3drs794728892
GWAS Ctlgrs794728892
Max Magnitude0
ClinVar
Risk rs794728892(A;A)
Alt rs794728892(A;A)
Reference rs794728892(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38592755C>T
CLNSRC
CLNACC RCV000183100.1,