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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
---|---|---|---|---|---|---|---|
View | NM_000540.3(RYR1):c.2677G>A (p.Gly893Ser) | Benign | RYR1-related myopathy | 2025-01-03 | 1.0 | ClinGen Congenital Myopathies Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for RYR1 Version 2.0.0 | RYR1 |
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