rs864309664

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs864309664(-;-)

Make rs864309664(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

65530716

Gene

SCYL1

is a	snp
is	mentioned by
dbSNP	rs864309664
dbSNP (classic)	rs864309664
ClinGen	rs864309664
ebi	rs864309664
HLI	rs864309664
Exac	rs864309664
Gnomad	rs864309664
Varsome	rs864309664
LitVar	rs864309664
Map	rs864309664
PheGenI	rs864309664
Biobank	rs864309664
1000 genomes	rs864309664
hgdp	rs864309664
ensembl	rs864309664
geneview	rs864309664
scholar	rs864309664
google	rs864309664
pharmgkb	rs864309664
gwascentral	rs864309664
openSNP	rs864309664
23andMe	rs864309664
SNPshot	rs864309664
SNPdbe	rs864309664
MSV3d	rs864309664
GWAS Ctlg	rs864309664

Max Magnitude

0

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,