Showing 1 to 1 of 1 rows
See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000162.5(GCK):c.1285A>C (p.Arg429=) | Likely Benign | monogenic diabetes | 2023-06-20 | 1.0 | ClinGen Monogenic Diabetes Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for GCK Version 1.1.0 | GCK |
Showing 1 to 1 of 1 rows