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rs794728918

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794728918(-;-)
Make rs794728918(-;C)
Make rs794728918(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38576680
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728918
ebirs794728918
HLIrs794728918
Exacrs794728918
Varsomers794728918
Maprs794728918
PheGenIrs794728918
hapmaprs794728918
1000 genomesrs794728918
hgdprs794728918
ensemblrs794728918
gopubmedrs794728918
geneviewrs794728918
scholarrs794728918
googlers794728918
pharmgkbrs794728918
gwascentralrs794728918
openSNPrs794728918
23andMers794728918
23andMe allrs794728918
SNP Nexus

SNPshotrs794728918
SNPdbers794728918
MSV3drs794728918
GWAS Ctlgrs794728918
Max Magnitude0
ClinVar
Risk rs794728918(C;C)
Alt rs794728918(C;C)
Reference rs794728918(;)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38618172dupG
CLNSRC
CLNACC RCV000183160.1,