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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
---|---|---|---|---|---|---|---|
View | NM_000314.8(PTEN):c.98T>C (p.Ile33Thr) | Uncertain Significance | PTEN hamartoma tumor syndrome | 2023-10-16 | 1.0 | ClinGen PTEN Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for PTEN Version 3.0.0 | PTEN |
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