ClinVar Miner

Submissions for variant NM_000081.4(LYST):c.4386G>A (p.Gly1462=)

dbSNP: rs1572270183
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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 RCV001430573 SCV001633315 likely benign Chédiak-Higashi syndrome 2018-06-30 criteria provided, single submitter clinical testing

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