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rs797046026

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797046026(-;-)
Make rs797046026(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position152401290
GeneSYNE1
is asnp
is mentioned by
dbSNPrs797046026
dbSNP (classic)rs797046026
ClinGenrs797046026
ebirs797046026
HLIrs797046026
Exacrs797046026
Gnomadrs797046026
Varsomers797046026
LitVarrs797046026
Maprs797046026
PheGenIrs797046026
Biobankrs797046026
1000 genomesrs797046026
hgdprs797046026
ensemblrs797046026
geneviewrs797046026
scholarrs797046026
googlers797046026
pharmgkbrs797046026
gwascentralrs797046026
openSNPrs797046026
23andMers797046026
SNPshotrs797046026
SNPdbers797046026
MSV3drs797046026
GWAS Ctlgrs797046026
Max Magnitude0
ClinVar
Risk rs797046026(-;-)
Alt rs797046026(-;-)
Reference Rs797046026(G;G)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene SYNE1
CLNDBN Spinocerebellar ataxia, autosomal recessive 8
Reversed 1
HGVS NC_000006.11:g.152722425delC
CLNSRC
CLNACC RCV000194453.1,