Showing 1 to 3 of 3 rows
See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_206933.2(USH2A):c.3902G>T (p.Gly1301Val) | Benign | Usher syndrome | 2024-04-01 | 2.1 | ClinGen Hearing Loss Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for CDH23, COCH, GJB2, KCNQ4, MYO6, MYO7A, SLC26A4, TECTA and USH2A Version 2 | USH2A |
| View | NM_206933.2(USH2A):c.3902G>T (p.Gly1301Val) | Benign | Usher syndrome | 2019-10-18 | 2.0 | - | USH2A |
| View | NM_206933.2(USH2A):c.3902G>T (p.Gly1301Val) | Benign | Usher syndrome type 2 | 2019-07-17 | 1.0 | - | USH2A |
Showing 1 to 3 of 3 rows