Showing 1 to 1 of 1 rows
See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
---|---|---|---|---|---|---|---|
View | NM_000545.8(HNF1A):c.1745A>G (p.His582Arg) | Likely Benign | monogenic diabetes | 2024-08-01 | 1.0 | ClinGen Monogenic Diabetes Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for HNF1A Version 2.1.0 | HNF1A |
Showing 1 to 1 of 1 rows