ClinVar Miner

Submissions for variant NM_033305.3(VPS13A):c.3468T>C (p.Ile1156=)

dbSNP: rs774438383
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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 RCV001446981 SCV001650036 likely benign not provided 2023-08-05 criteria provided, single submitter clinical testing

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