Multiple Sclerosis
An Unknown mode(s) within the Neurodegenerative disorders category
Candidate Gene Information
An Unknown mode(s) within the Neurodegenerative disorders category
Reported Pathogenic variants
| S.No. | Name/GeneID | Description | Cytogentic Band | Gene Location on genomic DNA | Gene Length | Exons | Details | Gene Cross-References |
| 1 | NR1H3/10062 | nuclear receptor subfamily 1 group H member 3 | 11p11.2 | Chr11, NC_000011.10 (47248300..47269033) |
20734 nt | 15 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: Orphanet GTR MedGen MalaCards EMBL-EBI OLS Monarch Initiative NORD | ||||||||
Patient care services
Clinical Symptoms & Disabilities
Prevalence
| Under development |