rs398124286
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(CAGA;CAGA) | 0 | common in clinvar |
Make rs398124286(-;-) |
Make rs398124286(-;CAGA) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 132277144 |
Gene | SETX |
is a | snp |
is | mentioned by |
dbSNP | rs398124286 |
dbSNP (classic) | rs398124286 |
ClinGen | rs398124286 |
ebi | rs398124286 |
HLI | rs398124286 |
Exac | rs398124286 |
Gnomad | rs398124286 |
Varsome | rs398124286 |
LitVar | rs398124286 |
Map | rs398124286 |
PheGenI | rs398124286 |
Biobank | rs398124286 |
1000 genomes | rs398124286 |
hgdp | rs398124286 |
ensembl | rs398124286 |
geneview | rs398124286 |
scholar | rs398124286 |
rs398124286 | |
pharmgkb | rs398124286 |
gwascentral | rs398124286 |
openSNP | rs398124286 |
23andMe | rs398124286 |
SNPshot | rs398124286 |
SNPdbe | rs398124286 |
MSV3d | rs398124286 |
GWAS Ctlg | rs398124286 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs398124286(-;-) |
Alt | rs398124286(-;-) |
Reference | Rs398124286(CAGA;CAGA) |
Significance | Pathogenic |
Disease | not provided Amyotrophic lateral sclerosis type 4 |
Variation | info |
Gene | SETX |
CLNDBN | not provided Amyotrophic lateral sclerosis type 4 |
Reversed | 1 |
HGVS | NC_000009.11:g.135152531_135152534delTCTG |
CLNSRC | HGMD |
CLNACC | RCV000081701.3, RCV000176318.1, |