ClinVar Miner

Submissions for variant NM_004329.3(BMPR1A):c.868+7A>G

dbSNP: rs1554890819
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001434076 SCV001636877 likely benign Juvenile polyposis syndrome 2023-03-15 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV001434076 SCV005406885 likely benign Juvenile polyposis syndrome 2024-08-05 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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