MEN1 (menin) germline pathogenic variant
Deterministic view of the source YAML entity. Clinical authority remains with the cited source IDs and reviewer sign-off state.
| ID | BIO-MEN1-GERMLINE |
|---|---|
| Type | Biomarker |
| Aliases | MEN1 (менін) germline патогенний варіантMEN1 germline pathogenic variant |
| Status | reviewed 2026-05-18 | pending_clinical_signoff |
| Diseases | None declared |
| Sources | SRC-NCCN-BCELL-2025 |
Biomarker Facts
| Biomarker type | gene_mutation |
|---|---|
| Mutation details | {"functional_impact": "loss_of_function", "gene": "MEN1", "gene_hugo_id": "HGNC:7010", "variant_type": "missense_or_truncating"} |
| Related biomarkers | None declared |
Notes
MEN1 germline — drives Multiple Endocrine Neoplasia type 1: primary hyperparathyroidism + pituitary adenomas + GEP-NETs (gastrinoma, insulinoma). STUB.
Used By
No reverse references found in the YAML corpus.