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rs794728919

From SNPedia

Orientationminus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs794728919(-;-)
Make rs794728919(-;GT)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38575445
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728919
ebirs794728919
HLIrs794728919
Exacrs794728919
Varsomers794728919
Maprs794728919
PheGenIrs794728919
hapmaprs794728919
1000 genomesrs794728919
hgdprs794728919
ensemblrs794728919
gopubmedrs794728919
geneviewrs794728919
scholarrs794728919
googlers794728919
pharmgkbrs794728919
gwascentralrs794728919
openSNPrs794728919
23andMers794728919
23andMe allrs794728919
SNP Nexus

SNPshotrs794728919
SNPdbers794728919
MSV3drs794728919
GWAS Ctlgrs794728919
Max Magnitude0
ClinVar
Risk rs794728919(;)
Alt rs794728919(;)
Reference rs794728919(GT;GT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38616936_38616937delAC
CLNSRC
CLNACC RCV000183161.2,