rs864309665

Orientation

plus

Stabilized

plus

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

Make rs864309665(-;-)

Make rs864309665(-;TG)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

65536075

Gene

SCYL1

is a	snp
is	mentioned by
dbSNP	rs864309665
dbSNP (classic)	rs864309665
ClinGen	rs864309665
ebi	rs864309665
HLI	rs864309665
Exac	rs864309665
Gnomad	rs864309665
Varsome	rs864309665
LitVar	rs864309665
Map	rs864309665
PheGenI	rs864309665
Biobank	rs864309665
1000 genomes	rs864309665
hgdp	rs864309665
ensembl	rs864309665
geneview	rs864309665
scholar	rs864309665
google	rs864309665
pharmgkb	rs864309665
gwascentral	rs864309665
openSNP	rs864309665
23andMe	rs864309665
SNPshot	rs864309665
SNPdbe	rs864309665
MSV3d	rs864309665
GWAS Ctlg	rs864309665

Max Magnitude

0

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,