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See Report
Preferred Variant Title
Classification
Condition
Published Date
Version
Criteria Specification
Gene
View NM_206933.3(USH2A):c.12295-3T>A
Pathogenic
Usher syndrome2023-02-06
2.0
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 2USH2A
View NM_206933.3(USH2A):c.12295-3T>A
Likely Pathogenic
Usher syndrome2019-10-23
1.0
-USH2A
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