ClinVar Miner

Submissions for variant NM_033305.3(VPS13A):c.1596-4G>T

dbSNP: rs1587392866
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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 RCV000950958 SCV001097303 likely benign not provided 2017-09-06 criteria provided, single submitter clinical testing

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