Showing 1 to 1 of 1 rows
See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000249.4(MLH1):c.2041G>C (p.Ala681Pro) | Uncertain Significance | Lynch syndrome 1 | 2024-10-11 | 1.0 | ClinGen InSiGHT Hereditary Colorectal Cancer/Polyposis Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for MLH1 Version 1.0.0 | MLH1 |
Showing 1 to 1 of 1 rows