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rs794727794

From SNPedia

Orientationminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs794727794(-;-)
Make rs794727794(-;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position94603343
GeneCASD1, SGCE
is asnp
is mentioned by
dbSNPrs794727794
ebirs794727794
HLIrs794727794
Exacrs794727794
Varsomers794727794
Maprs794727794
PheGenIrs794727794
hapmaprs794727794
1000 genomesrs794727794
hgdprs794727794
ensemblrs794727794
gopubmedrs794727794
geneviewrs794727794
scholarrs794727794
googlers794727794
pharmgkbrs794727794
gwascentralrs794727794
openSNPrs794727794
23andMers794727794
23andMe allrs794727794
SNP Nexus

SNPshotrs794727794
SNPdbers794727794
MSV3drs794727794
GWAS Ctlgrs794727794
Max Magnitude0
ClinVar
Risk rs794727794(;)
Alt rs794727794(;)
Reference rs794727794(AT;AT)
Significance Pathogenic
Disease Myoclonic dystonia
Variation info
Gene SGCE
CLNDBN Myoclonic dystonia
Reversed 1
HGVS NC_000007.13:g.94232655_94232656delAT
CLNSRC
CLNACC RCV000179425.1,