ClinVar Miner

Submissions for variant NM_016032.4(ZDHHC9):c.332C>T (p.Ala111Val)

dbSNP: rs1556006489
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000646764 SCV000768549 likely benign Syndromic X-linked intellectual disability Raymond type 2023-10-03 criteria provided, single submitter clinical testing

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