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rs794728876

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728876(G;G)
Make rs794728876(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38575313
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728876
ebirs794728876
HLIrs794728876
Exacrs794728876
Varsomers794728876
Maprs794728876
PheGenIrs794728876
hapmaprs794728876
1000 genomesrs794728876
hgdprs794728876
ensemblrs794728876
gopubmedrs794728876
geneviewrs794728876
scholarrs794728876
googlers794728876
pharmgkbrs794728876
gwascentralrs794728876
openSNPrs794728876
23andMers794728876
23andMe allrs794728876
SNP Nexus

SNPshotrs794728876
SNPdbers794728876
MSV3drs794728876
GWAS Ctlgrs794728876
Max Magnitude0
ClinVar
Risk rs794728876(G;G)
Alt rs794728876(G;G)
Reference rs794728876(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38616804A>C
CLNSRC
CLNACC RCV000183041.2,