ClinVar Miner

Submissions for variant NM_152383.5(DIS3L2):c.781C>T (p.Leu261=)

dbSNP: rs1553610364
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000638537 SCV000760061 likely benign Perlman syndrome 2017-11-20 criteria provided, single submitter clinical testing

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