ClinVar Miner

Submissions for variant NM_153717.3(EVC):c.2328G>C (p.Val776=)

dbSNP: rs913233513
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001427123 SCV001629796 likely benign Ellis-van Creveld syndrome; Curry-Hall syndrome 2022-11-10 criteria provided, single submitter clinical testing

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