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See Report
Preferred Variant Title
Classification
Condition
Published Date
Version
Criteria Specification
Gene
View NM_000314.8(PTEN):c.892C>G (p.Gln298Glu)
Likely Benign
PTEN hamartoma tumor syndrome2023-10-19
2.0
ClinGen PTEN Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for PTEN Version 3.0.0PTEN
View NM_000314.6(PTEN):c.892C>G (p.Gln298Glu)
Uncertain Significance
PTEN hamartoma tumor syndrome2019-07-23
1.0
-PTEN
Showing 1 to 2 of 2 rows