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rs794728867

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728867(C;C)
Make rs794728867(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38585762
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728867
ebirs794728867
HLIrs794728867
Exacrs794728867
Varsomers794728867
Maprs794728867
PheGenIrs794728867
hapmaprs794728867
1000 genomesrs794728867
hgdprs794728867
ensemblrs794728867
gopubmedrs794728867
geneviewrs794728867
scholarrs794728867
googlers794728867
pharmgkbrs794728867
gwascentralrs794728867
openSNPrs794728867
23andMers794728867
23andMe allrs794728867
SNP Nexus

SNPshotrs794728867
SNPdbers794728867
MSV3drs794728867
GWAS Ctlgrs794728867
Max Magnitude0
ClinVar
Risk rs794728867(C;C)
Alt rs794728867(C;C)
Reference rs794728867(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38627253A>G
CLNSRC
CLNACC RCV000183010.1,