ClinVar Miner

Submissions for variant NM_001204.7(BMPR2):c.1761T>G (p.Ile587Met)

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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 RCV005030812 SCV005654576 uncertain significance Pulmonary hypertension, primary, 1; Pulmonary venoocclusive disease 1 2024-04-25 criteria provided, single submitter clinical testing

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