rs28941475

Orientation

minus

Stabilized

minus

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

Make rs28941475(C;T)

Make rs28941475(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

132349421

Gene

SETX

is a	snp
is	mentioned by
dbSNP	rs28941475
dbSNP (classic)	rs28941475
ClinGen	rs28941475
ebi	rs28941475
HLI	rs28941475
Exac	rs28941475
Gnomad	rs28941475
Varsome	rs28941475
LitVar	rs28941475
Map	rs28941475
PheGenI	rs28941475
Biobank	rs28941475
1000 genomes	rs28941475
hgdp	rs28941475
ensembl	rs28941475
geneview	rs28941475
scholar	rs28941475
google	rs28941475
pharmgkb	rs28941475
gwascentral	rs28941475
openSNP	rs28941475
23andMe	rs28941475
SNPshot	rs28941475
SNPdbe	rs28941475
MSV3d	rs28941475
GWAS Ctlg	rs28941475

Max Magnitude

0

OMIM	608465
Desc	AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE
Variant	0007
Related	also

ClinVar
Risk	rs28941475(T;T)
Alt	rs28941475(T;T)
Reference	Rs28941475(C;C)
Significance	Pathogenic
Disease	Amyotrophic lateral sclerosis type 4 not provided
Variation	info
Gene	SETX
CLNDBN	Amyotrophic lateral sclerosis type 4 not provided
Reversed	1
HGVS	NC_000009.11:g.135224808G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000002380.5, RCV000414273.1,