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

rs864309667

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309667(C;T)
Make rs864309667(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position65536319
GeneSCYL1
is asnp
is mentioned by
dbSNPrs864309667
ebirs864309667
HLIrs864309667
Exacrs864309667
Varsomers864309667
Maprs864309667
PheGenIrs864309667
hapmaprs864309667
1000 genomesrs864309667
hgdprs864309667
ensemblrs864309667
gopubmedrs864309667
geneviewrs864309667
scholarrs864309667
googlers864309667
pharmgkbrs864309667
gwascentralrs864309667
openSNPrs864309667
23andMers864309667
23andMe allrs864309667
SNP Nexus

SNPshotrs864309667
SNPdbers864309667
MSV3drs864309667
GWAS Ctlgrs864309667
Max Magnitude0
ClinVar
Risk rs864309667(T;T)
Alt rs864309667(T;T)
Reference rs864309667(C;C)
Significance Pathogenic
Disease Spinocerebellar ataxia 21
Variation info
Gene SCYL1
CLNDBN Spinocerebellar ataxia 21
Reversed 0
HGVS NC_000011.9:g.65303790C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000203251.2,