The ClinGen Evidence Repository is an FDA-recognized human genetic variant database containing expert-curated assertions regarding variants' pathogenicity and supporting evidence summaries.
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Curation History
Variant: CA132255 43186
VCEP: Hearing Loss VCEP
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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000260.4(MYO7A):c.2558G>A (p.Arg853His) | Likely Pathogenic | nonsyndromic genetic deafness | 2023-01-25 | 1.3 | 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 | MYO7A |
| View | NM_000260.4(MYO7A):c.2558G>A (p.Arg853His) | Likely Pathogenic | nonsyndromic genetic deafness | 2019-12-18 | 1.2 | - | MYO7A |
| View | NM_000260.4(MYO7A):c.2558G>A (p.Arg853His) | Likely Pathogenic | nonsyndromic genetic deafness | 2019-12-18 | 1.1 | - | MYO7A |
| View | NM_000260.4(MYO7A):c.2558G>A (p.Arg853His) | Likely Pathogenic | nonsyndromic genetic deafness | 2019-10-29 | 1.0 | - | MYO7A |
Showing 1 to 4 of 4 rows