ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.-868G>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005049885 SCV005678966 uncertain significance Macrocephaly-autism syndrome; Familial meningioma; Glioma susceptibility 2; Familial prostate cancer; Cowden syndrome 1 2024-03-05 criteria provided, single submitter clinical testing

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