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rs794728909

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728909(-;-)
Make rs794728909(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38587493
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728909
ebirs794728909
HLIrs794728909
Exacrs794728909
Varsomers794728909
Maprs794728909
PheGenIrs794728909
hapmaprs794728909
1000 genomesrs794728909
hgdprs794728909
ensemblrs794728909
gopubmedrs794728909
geneviewrs794728909
scholarrs794728909
googlers794728909
pharmgkbrs794728909
gwascentralrs794728909
openSNPrs794728909
23andMers794728909
23andMe allrs794728909
SNP Nexus

SNPshotrs794728909
SNPdbers794728909
MSV3drs794728909
GWAS Ctlgrs794728909
Max Magnitude0
ClinVar
Risk rs794728909(;)
Alt rs794728909(;)
Reference rs794728909(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38628984delC
CLNSRC
CLNACC RCV000183148.1,