ClinVar Miner

Submissions for variant NM_001567.4(INPPL1):c.1108_1155del (p.Ser370_Lys385del)

dbSNP: rs1565388201
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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, Cologne University RCV000722107 SCV000853269 uncertain significance Opsismodysplasia no assertion criteria provided clinical testing

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