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: CA387461043 449488
VCEP: Hearing Loss VCEP
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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_004004.6(GJB2):c.488T>C (p.Met163Thr) | Uncertain Significance | nonsyndromic genetic deafness | 2025-01-06 | 1.1 | 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 | GJB2 |
| View | NM_004004.6(GJB2):c.488T>C (p.Met163Thr) | Uncertain Significance | nonsyndromic genetic deafness | 2020-04-30 | 1.0 | - | GJB2 |
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