ClinVar Miner

Submissions for variant NM_000322.5(PRPH2):c.466A>G (p.Ile156Val)

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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 RCV004817712 SCV005070984 uncertain significance Retinal dystrophy 2017-01-01 no assertion criteria provided clinical testing

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