ClinVar Miner

Submissions for variant NM_025132.4(WDR19):c.670G>C (p.Asp224His)

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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 RCV005027348 SCV005662195 uncertain significance Asphyxiating thoracic dystrophy 5; Nephronophthisis 13; Cranioectodermal dysplasia 4; Senior-Loken syndrome 8; Spermatogenic failure 72 2024-04-12 criteria provided, single submitter clinical testing

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