ClinVar Miner

Submissions for variant NM_144670.6(A2ML1):c.3294T>G (p.Thr1098=)

dbSNP: rs764429289
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001290601 SCV001478693 likely benign not specified 2021-01-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001480619 SCV001684942 likely benign not provided 2021-10-27 criteria provided, single submitter clinical testing

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