ClinVar Miner

Submissions for variant NM_002691.4(POLD1):c.1776-53G>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005028703 SCV005650301 uncertain significance Colorectal cancer, susceptibility to, 10; Mandibular hypoplasia-deafness-progeroid syndrome; Immunodeficiency 120 2024-03-28 criteria provided, single submitter clinical testing

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