ClinVar Miner

Submissions for variant NM_004329.3(BMPR1A):c.1424G>T (p.Cys475Phe)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004012420 SCV004837652 uncertain significance Juvenile polyposis syndrome 2023-11-30 criteria provided, single submitter clinical testing
Baylor Genetics RCV004573456 SCV005058176 uncertain significance Polyposis syndrome, hereditary mixed, 2 2024-01-26 criteria provided, single submitter clinical testing

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