rs750331613

Orientation

plus

Stabilized

plus

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

Make rs750331613(C;T)

Make rs750331613(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

93515346

Gene

GRID2

is a	snp
is	mentioned by
dbSNP	rs750331613
dbSNP (classic)	rs750331613
ClinGen	rs750331613
ebi	rs750331613
HLI	rs750331613
Exac	rs750331613
Gnomad	rs750331613
Varsome	rs750331613
LitVar	rs750331613
Map	rs750331613
PheGenI	rs750331613
Biobank	rs750331613
1000 genomes	rs750331613
hgdp	rs750331613
ensembl	rs750331613
geneview	rs750331613
scholar	rs750331613
google	rs750331613
pharmgkb	rs750331613
gwascentral	rs750331613
openSNP	rs750331613
23andMe	rs750331613
SNPshot	rs750331613
SNPdbe	rs750331613
MSV3d	rs750331613
GWAS Ctlg	rs750331613

Max Magnitude

0

ClinVar
Risk	rs750331613(T;T)
Alt	rs750331613(T;T)
Reference	Rs750331613(C;C)
Significance	Pathogenic
Disease	Spinocerebellar ataxia
Variation	info
Gene	GRID2
CLNDBN	Spinocerebellar ataxia, autosomal recessive 18
Reversed	0
HGVS	NC_000004.11:g.94436497C>T
CLNSRC
CLNACC	RCV000490816.1,