ClinVar Miner

Submissions for variant NM_031220.4(PITPNM3):c.1381C>G (p.Pro461Ala)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg RCV004815970 SCV005070399 uncertain significance Retinal dystrophy 2023-01-01 no assertion criteria provided clinical testing

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