ClinVar Miner

Submissions for variant NM_144773.4(PROKR2):c.819G>T (p.Thr273=)

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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 RCV002952493 SCV003268039 likely benign not provided 2022-08-09 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002952493 SCV004149839 likely benign not provided 2022-12-01 criteria provided, single submitter clinical testing PROKR2: BP4, BP7

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