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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
---|---|---|---|---|---|---|---|
View | NM_000337.6(SGCD):c.191T>C (p.Ile64Thr) | Uncertain Significance | autosomal recessive limb-girdle muscular dystrophy | 2025-01-08 | 1.0 | ClinGen Limb Girdle Muscular Dystrophy Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for SGCD Version 1.0.0 | SGCD |
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