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rs864309666

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309666(A;A)
Make rs864309666(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position65532806
GeneSCYL1
is asnp
is mentioned by
dbSNPrs864309666
ebirs864309666
HLIrs864309666
Exacrs864309666
Varsomers864309666
Maprs864309666
PheGenIrs864309666
hapmaprs864309666
1000 genomesrs864309666
hgdprs864309666
ensemblrs864309666
gopubmedrs864309666
geneviewrs864309666
scholarrs864309666
googlers864309666
pharmgkbrs864309666
gwascentralrs864309666
openSNPrs864309666
23andMers864309666
23andMe allrs864309666
SNP Nexus

SNPshotrs864309666
SNPdbers864309666
MSV3drs864309666
GWAS Ctlgrs864309666
Max Magnitude0
ClinVar
Risk rs864309666(A;A)
Alt rs864309666(A;A)
Reference rs864309666(G;G)
Significance Pathogenic
Disease Spinocerebellar ataxia 21
Variation info
Gene SCYL1
CLNDBN Spinocerebellar ataxia 21
Reversed 0
HGVS NC_000011.9:g.65300277G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000203250.1,