rs398123258
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;C) | 3 | Carrier of a mucopolysaccharidosis type 1 mutation |
(C;C) | 0 | common in clinvar |
Make rs398123258(-;-) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 1004083 |
Gene | IDUA |
is a | snp |
is | mentioned by |
dbSNP | rs398123258 |
dbSNP (classic) | rs398123258 |
ClinGen | rs398123258 |
ebi | rs398123258 |
HLI | rs398123258 |
Exac | rs398123258 |
Gnomad | rs398123258 |
Varsome | rs398123258 |
LitVar | rs398123258 |
Map | rs398123258 |
PheGenI | rs398123258 |
Biobank | rs398123258 |
1000 genomes | rs398123258 |
hgdp | rs398123258 |
ensembl | rs398123258 |
geneview | rs398123258 |
scholar | rs398123258 |
rs398123258 | |
pharmgkb | rs398123258 |
gwascentral | rs398123258 |
openSNP | rs398123258 |
23andMe | rs398123258 |
SNPshot | rs398123258 |
SNPdbe | rs398123258 |
MSV3d | rs398123258 |
GWAS Ctlg | rs398123258 |
Max Magnitude | 3 |
ClinVar | |
---|---|
Risk | rs398123258(-;-) |
Alt | rs398123258(-;-) |
Reference | Rs398123258(C;C) |
Significance | Pathogenic |
Disease | not provided Hurler syndrome |
Variation | info |
Gene | IDUA |
CLNDBN | not provided Hurler syndrome |
Reversed | 0 |
HGVS | NC_000004.11:g.997871delC |
CLNSRC | ClinVar |
CLNACC | RCV000078385.3, RCV000174452.2, |