ClinVar Miner

Submissions for variant NM_033056.4(PCDH15):c.3450C>T (p.Ile1150=) (rs146374856)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000928337 SCV001073947 likely benign not provided 2020-10-27 criteria provided, single submitter clinical testing
GeneDx RCV000928337 SCV001784656 likely benign not provided 2020-11-06 criteria provided, single submitter clinical testing
Natera, Inc. RCV001273389 SCV001456420 likely benign Usher syndrome type 1F 2020-01-10 no assertion criteria provided clinical testing

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