ClinVar Miner

Submissions for variant NM_004311.4(ARL3):c.99T>G (p.Leu33=)

dbSNP: rs2136008697
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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 RCV001411971 SCV001614043 likely benign not provided 2022-03-10 criteria provided, single submitter clinical testing

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