ClinVar Miner

Submissions for variant NM_147127.5(EVC2):c.2710C>T (p.Gln904Ter)

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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 RCV005027359 SCV005658240 pathogenic Ellis-van Creveld syndrome; Curry-Hall syndrome 2024-03-29 criteria provided, single submitter clinical testing

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