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rs794728920

From SNPedia

Orientationminus
Geno Mag Summary
(ATC;ATC) 0 common in clinvar
Make rs794728920(-;-)
Make rs794728920(-;ATC)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38575327
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728920
ebirs794728920
HLIrs794728920
Exacrs794728920
Varsomers794728920
Maprs794728920
PheGenIrs794728920
hapmaprs794728920
1000 genomesrs794728920
hgdprs794728920
ensemblrs794728920
gopubmedrs794728920
geneviewrs794728920
scholarrs794728920
googlers794728920
pharmgkbrs794728920
gwascentralrs794728920
openSNPrs794728920
23andMers794728920
23andMe allrs794728920
SNP Nexus

SNPshotrs794728920
SNPdbers794728920
MSV3drs794728920
GWAS Ctlgrs794728920
Max Magnitude0
ClinVar
Risk rs794728920(;)
Alt rs794728920(;)
Reference rs794728920(ATC;ATC)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38616818_38616820delGAT
CLNSRC
CLNACC RCV000183162.1,