ClinVar Miner

Submissions for variant NM_031885.5(BBS2):c.718-10T>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 RCV005015637 SCV005644056 uncertain significance Bardet-Biedl syndrome 2; Retinitis pigmentosa 74 2024-04-12 criteria provided, single submitter clinical testing

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