rs730882209

Orientation

minus

Stabilized

minus

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

Make rs730882209(-;G)

Make rs730882209(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

9

Position

132326375

Gene

SETX

is a	snp
is	mentioned by
dbSNP	rs730882209
dbSNP (classic)	rs730882209
ClinGen	rs730882209
ebi	rs730882209
HLI	rs730882209
Exac	rs730882209
Gnomad	rs730882209
Varsome	rs730882209
LitVar	rs730882209
Map	rs730882209
PheGenI	rs730882209
Biobank	rs730882209
1000 genomes	rs730882209
hgdp	rs730882209
ensembl	rs730882209
geneview	rs730882209
scholar	rs730882209
google	rs730882209
pharmgkb	rs730882209
gwascentral	rs730882209
openSNP	rs730882209
23andMe	rs730882209
SNPshot	rs730882209
SNPdbe	rs730882209
MSV3d	rs730882209
GWAS Ctlg	rs730882209

Max Magnitude

0

ClinVar
Risk	rs730882209(G;G)
Alt	rs730882209(G;G)
Reference	Rs730882209(-;-)
Significance	Probable-Pathogenic
Disease	Ataxia Cerebellar atrophy Dysdiadochokinesis Dysmetria Nystagmus Slightly reduced reflexes Slurred speech
Variation	info
Gene	SETX
CLNDBN	Ataxia Cerebellar atrophy Dysdiadochokinesis Dysmetria Nystagmus Slightly reduced reflexes Slurred speech
Reversed	1
HGVS	NC_000009.11:g.135201763dupC
CLNSRC	King Faisal Specialist Hospital and Research Center
CLNACC	RCV000162115.1,