rs74315458
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs74315458(A;A) |
Make rs74315458(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 50627374 |
Gene | ARSA |
is a | snp |
is | mentioned by |
dbSNP | rs74315458 |
dbSNP (classic) | rs74315458 |
ClinGen | rs74315458 |
ebi | rs74315458 |
HLI | rs74315458 |
Exac | rs74315458 |
Gnomad | rs74315458 |
Varsome | rs74315458 |
LitVar | rs74315458 |
Map | rs74315458 |
PheGenI | rs74315458 |
Biobank | rs74315458 |
1000 genomes | rs74315458 |
hgdp | rs74315458 |
ensembl | rs74315458 |
geneview | rs74315458 |
scholar | rs74315458 |
rs74315458 | |
pharmgkb | rs74315458 |
gwascentral | rs74315458 |
openSNP | rs74315458 |
23andMe | rs74315458 |
SNPshot | rs74315458 |
SNPdbe | rs74315458 |
MSV3d | rs74315458 |
GWAS Ctlg | rs74315458 |
Max Magnitude | 0 |
aka c.257G>A (p.Arg86Gln)
23andMe name: i5004781
ClinVar | |
---|---|
Risk | rs74315458(A;A) |
Alt | rs74315458(A;A) |
Reference | Rs74315458(G;G) |
Significance | Pathogenic |
Disease | Metachromatic leukodystrophy Metachromatic leukodystrophy |
Variation | info |
Gene | ARSA |
CLNDBN | Metachromatic leukodystrophy, late-onset Metachromatic leukodystrophy |
Reversed | 1 |
HGVS | NC_000022.10:g.51065802C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000003205.2, RCV000020316.2, |
[PMID 1353340] Late-onset metachromatic leukodystrophy: molecular pathology in two siblings.
[PMID 15720392] Missense mutations as a cause of metachromatic leukodystrophy. Degradation of arylsulfatase A in the endoplasmic reticulum.