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rs794728912

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728912(-;-)
Make rs794728912(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38585945
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728912
ebirs794728912
HLIrs794728912
Exacrs794728912
Varsomers794728912
Maprs794728912
PheGenIrs794728912
hapmaprs794728912
1000 genomesrs794728912
hgdprs794728912
ensemblrs794728912
gopubmedrs794728912
geneviewrs794728912
scholarrs794728912
googlers794728912
pharmgkbrs794728912
gwascentralrs794728912
openSNPrs794728912
23andMers794728912
23andMe allrs794728912
SNP Nexus

SNPshotrs794728912
SNPdbers794728912
MSV3drs794728912
GWAS Ctlgrs794728912
Max Magnitude0
ClinVar
Risk rs794728912(;)
Alt rs794728912(;)
Reference rs794728912(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38627436delC
CLNSRC
CLNACC RCV000183153.2,