Showing 1 to 2 of 2 rows
See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_194248.3(OTOF):c.4463A>T (p.Asp1488Val) | Uncertain Significance | nonsyndromic genetic deafness | 2025-03-28 | 1.1 | ClinGen Hearing Loss Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for OTOF and MYO15A Version 1 | OTOF |
| View | NM_194248.3(OTOF):c.4463A>T (p.Asp1488Val) | Uncertain Significance | nonsyndromic genetic deafness | 2022-05-13 | 1.0 | - | OTOF |
Showing 1 to 2 of 2 rows