ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.3075G>C (p.Thr1025=)

dbSNP: rs141637316
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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 RCV003045221 SCV003320947 likely benign Cohen syndrome 2022-03-02 criteria provided, single submitter clinical testing

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