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rs794726859

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794726859(A;A)
Make rs794726859(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position11017342
GeneSLC6A1, SLC6A1-AS1
is asnp
is mentioned by
dbSNPrs794726859
ebirs794726859
HLIrs794726859
Exacrs794726859
Varsomers794726859
Maprs794726859
PheGenIrs794726859
hapmaprs794726859
1000 genomesrs794726859
hgdprs794726859
ensemblrs794726859
gopubmedrs794726859
geneviewrs794726859
scholarrs794726859
googlers794726859
pharmgkbrs794726859
gwascentralrs794726859
openSNPrs794726859
23andMers794726859
23andMe allrs794726859
SNP Nexus

SNPshotrs794726859
SNPdbers794726859
MSV3drs794726859
GWAS Ctlgrs794726859
Max Magnitude0
ClinVar
Risk rs794726859(A;A)
Alt rs794726859(A;A)
Reference rs794726859(G;G)
Significance Pathogenic
Disease Myoclonic-atonic epilepsy
Variation info
Gene SLC6A1-AS1 SLC6A1
CLNDBN Myoclonic-atonic epilepsy
Reversed 0
HGVS NC_000003.11:g.11059028G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000172994.2,