ClinVar Miner

Submissions for variant NM_174878.3(CLRN1):c.434-2A>T

dbSNP: rs1576623563
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet RCV000787816 SCV000926827 likely pathogenic Retinitis pigmentosa 2018-04-01 no assertion criteria provided research

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