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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_206933.2(USH2A):c.12505A>G (p.Thr4169Ala) | Likely Benign | Usher syndrome | 2019-10-18 | 2.0 | - | USH2A |
| View | NM_206933.2(USH2A):c.12505A>G (p.Thr4169Ala) | Likely Benign | Usher syndrome type 2 | 2019-07-17 | 1.0 | - | USH2A |
Showing 1 to 2 of 2 rows