rs864309667

Orientation

plus

Stabilized

plus

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

Make rs864309667(C;T)

Make rs864309667(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

65536319

Gene

SCYL1

is a	snp
is	mentioned by
dbSNP	rs864309667
dbSNP (classic)	rs864309667
ClinGen	rs864309667
ebi	rs864309667
HLI	rs864309667
Exac	rs864309667
Gnomad	rs864309667
Varsome	rs864309667
LitVar	rs864309667
Map	rs864309667
PheGenI	rs864309667
Biobank	rs864309667
1000 genomes	rs864309667
hgdp	rs864309667
ensembl	rs864309667
geneview	rs864309667
scholar	rs864309667
google	rs864309667
pharmgkb	rs864309667
gwascentral	rs864309667
openSNP	rs864309667
23andMe	rs864309667
SNPshot	rs864309667
SNPdbe	rs864309667
MSV3d	rs864309667
GWAS Ctlg	rs864309667

Max Magnitude

0

ClinVar
Risk	rs864309667(T;T)
Alt	rs864309667(T;T)
Reference	Rs864309667(C;C)
Significance	Pathogenic
Disease	Spinocerebellar ataxia 21
Variation	info
Gene	SCYL1
CLNDBN	Spinocerebellar ataxia 21
Reversed	0
HGVS	NC_000011.9:g.65303790C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000203251.2,