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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_024675.3(PALB2):c.871G>A (p.Ala291Thr) | Uncertain Significance | PALB2-related cancer predisposition | 2025-09-16 | 2.0 | ClinGen Hereditary Breast, Ovarian and Pancreatic Cancer Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for PALB2 Version 1.0.0 | PALB2 |
| View | NM_024675.3(PALB2):c.871G>A (p.Ala291Thr) | Uncertain Significance | hereditary breast cancer | 2023-04-07 | 1.0 | ClinGen Hereditary Breast, Ovarian and Pancreatic Cancer Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for PALB2 Version 1.0.0 | PALB2 |
Showing 1 to 2 of 2 rows