Have questions? Visit https://www.reddit.com/r/SNPedia

rs797046025

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797046025(C;T)
Make rs797046025(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position152143733
GeneSYNE1
is asnp
is mentioned by
dbSNPrs797046025
ebirs797046025
HLIrs797046025
Exacrs797046025
Varsomers797046025
Maprs797046025
PheGenIrs797046025
hapmaprs797046025
1000 genomesrs797046025
hgdprs797046025
ensemblrs797046025
gopubmedrs797046025
geneviewrs797046025
scholarrs797046025
googlers797046025
pharmgkbrs797046025
gwascentralrs797046025
openSNPrs797046025
23andMers797046025
23andMe allrs797046025
SNP Nexus

SNPshotrs797046025
SNPdbers797046025
MSV3drs797046025
GWAS Ctlgrs797046025
Max Magnitude0
ClinVar
Risk rs797046025(T;T)
Alt rs797046025(T;T)
Reference rs797046025(C;C)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene SYNE1
CLNDBN Spinocerebellar ataxia, autosomal recessive 8
Reversed 1
HGVS NC_000006.11:g.152464868G>A
CLNSRC
CLNACC RCV000194323.1,