rs1056899

Orientation

minus

Stabilized

minus

Make rs1056899(A;A)

Make rs1056899(A;G)

Make rs1056899(G;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

132264514

Gene

SETX

is a	snp
is	mentioned by
dbSNP	rs1056899
dbSNP (classic)	rs1056899
ClinGen	rs1056899
ebi	rs1056899
HLI	rs1056899
Exac	rs1056899
Gnomad	rs1056899
Varsome	rs1056899
LitVar	rs1056899
Map	rs1056899
PheGenI	rs1056899
Biobank	rs1056899
1000 genomes	rs1056899
hgdp	rs1056899
ensembl	rs1056899
geneview	rs1056899
scholar	rs1056899
google	rs1056899
pharmgkb	rs1056899
gwascentral	rs1056899
openSNP	rs1056899
23andMe	rs1056899
SNPshot	rs1056899
SNPdbe	rs1056899
MSV3d	rs1056899
GWAS Ctlg	rs1056899

GMAF

0.4908

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

ClinVar
Risk	rs1056899(G;G)
Alt	rs1056899(G;G)
Reference	rs1056899(A;A)
Significance	Other
Disease	not specified Ataxia with Oculomotor Apraxia Amyotrophic Lateral Sclerosis
Variation	info
Gene	SETX
CLNDBN	not specified Ataxia with Oculomotor Apraxia Amyotrophic Lateral Sclerosis, Dominant
Reversed	1
HGVS	NC_000009.11:g.135139901T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000081702.9, RCV000294610.1, RCV000388921.1,