ClinVar Miner

Submissions for variant NM_004329.2(BMPR1A):c.993G>A (p.Leu331=) (rs786202827)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000165844 SCV000216592 likely benign Hereditary cancer-predisposing syndrome 2014-09-29 criteria provided, single submitter clinical testing
Counsyl RCV000412325 SCV000488953 likely benign Juvenile polyposis syndrome 2016-07-25 criteria provided, single submitter clinical testing

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