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rs794728895

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728895(G;T)
Make rs794728895(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38551141
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728895
ebirs794728895
HLIrs794728895
Exacrs794728895
Varsomers794728895
Maprs794728895
PheGenIrs794728895
hapmaprs794728895
1000 genomesrs794728895
hgdprs794728895
ensemblrs794728895
gopubmedrs794728895
geneviewrs794728895
scholarrs794728895
googlers794728895
pharmgkbrs794728895
gwascentralrs794728895
openSNPrs794728895
23andMers794728895
23andMe allrs794728895
SNP Nexus

SNPshotrs794728895
SNPdbers794728895
MSV3drs794728895
GWAS Ctlgrs794728895
Max Magnitude0
ClinVar
Risk rs794728895(T;T)
Alt rs794728895(T;T)
Reference rs794728895(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38592632C>A
CLNSRC
CLNACC RCV000183110.1,