rs80358242
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs80358242(A;A) |
Make rs80358242(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 50084727 |
Gene | MLC1 |
is a | snp |
is | mentioned by |
dbSNP | rs80358242 |
dbSNP (classic) | rs80358242 |
ClinGen | rs80358242 |
ebi | rs80358242 |
HLI | rs80358242 |
Exac | rs80358242 |
Gnomad | rs80358242 |
Varsome | rs80358242 |
LitVar | rs80358242 |
Map | rs80358242 |
PheGenI | rs80358242 |
Biobank | rs80358242 |
1000 genomes | rs80358242 |
hgdp | rs80358242 |
ensembl | rs80358242 |
geneview | rs80358242 |
scholar | rs80358242 |
rs80358242 | |
pharmgkb | rs80358242 |
gwascentral | rs80358242 |
openSNP | rs80358242 |
23andMe | rs80358242 |
SNPshot | rs80358242 |
SNPdbe | rs80358242 |
MSV3d | rs80358242 |
GWAS Ctlg | rs80358242 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs80358242(A;A) |
Alt | rs80358242(A;A) |
Reference | Rs80358242(G;G) |
Significance | Pathogenic |
Disease | Megalencephalic leukoencephalopathy with subcortical cysts 1 not provided |
Variation | info |
Gene | MLC1 |
CLNDBN | Megalencephalic leukoencephalopathy with subcortical cysts 1 not provided |
Reversed | 1 |
HGVS | NC_000022.10:g.50523156C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000004986.4, RCV000293896.1, |
[PMID 12189496] Megalencephalic leukoencephalopathy with subcortical cysts; a founder effect in Israeli patients and a higher than expected carrier rate among Libyan Jews.