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rs864309664

From SNPedia

Orientationplus
Make rs864309664(-;-)
Make rs864309664(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position65530716
GeneSCYL1
is asnp
is mentioned by
dbSNPrs864309664
ebirs864309664
HLIrs864309664
Exacrs864309664
Varsomers864309664
Maprs864309664
PheGenIrs864309664
hapmaprs864309664
1000 genomesrs864309664
hgdprs864309664
ensemblrs864309664
gopubmedrs864309664
geneviewrs864309664
scholarrs864309664
googlers864309664
pharmgkbrs864309664
gwascentralrs864309664
openSNPrs864309664
23andMers864309664
23andMe allrs864309664
SNP Nexus

SNPshotrs864309664
SNPdbers864309664
MSV3drs864309664
GWAS Ctlgrs864309664
Max Magnitude
ClinVar
Risk rs864309664(;)
Alt rs864309664(;)
Reference rs864309664(G;G)
Significance Pathogenic
Disease Spinocerebellar ataxia 21
Variation info
Gene SCYL1
CLNDBN Spinocerebellar ataxia 21
Reversed 0
HGVS NC_000011.9:g.65298187delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000203252.1,