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rs864309665

From SNPedia

Orientationplus
Make rs864309665(-;-)
Make rs864309665(-;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position65536075
GeneSCYL1
is asnp
is mentioned by
dbSNPrs864309665
ebirs864309665
HLIrs864309665
Exacrs864309665
Varsomers864309665
Maprs864309665
PheGenIrs864309665
hapmaprs864309665
1000 genomesrs864309665
hgdprs864309665
ensemblrs864309665
gopubmedrs864309665
geneviewrs864309665
scholarrs864309665
googlers864309665
pharmgkbrs864309665
gwascentralrs864309665
openSNPrs864309665
23andMers864309665
23andMe allrs864309665
SNP Nexus

SNPshotrs864309665
SNPdbers864309665
MSV3drs864309665
GWAS Ctlgrs864309665
Max Magnitude
ClinVar
Risk rs864309665(;)
Alt rs864309665(;)
Reference rs864309665(TG;TG)
Significance Pathogenic
Disease Spinocerebellar ataxia 21
Variation info
Gene SCYL1
CLNDBN Spinocerebellar ataxia 21
Reversed 0
HGVS NC_000011.9:g.65303546_65303547delTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000203253.1,