ClinVar Miner

Submissions for variant NM_139076.3(ABRAXAS1):c.496T>C (p.Leu166=)

dbSNP: rs1060504866
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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 RCV000468182 SCV000562563 likely benign not provided 2016-10-03 criteria provided, single submitter clinical testing

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