ClinVar Miner

Submissions for variant NM_033305.3(VPS13A):c.7446G>T (p.Gly2482=)

dbSNP: rs748257173
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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 RCV001419162 SCV001621409 likely benign not provided 2023-07-27 criteria provided, single submitter clinical testing

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