ClinVar Miner

Submissions for variant NM_024101.7(MLPH):c.1710G>A (p.Val570=)

gnomAD frequency: 0.00198  dbSNP: rs41270745
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000889302 SCV001032974 benign not provided 2024-01-15 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001700497 SCV002070861 likely benign not specified 2019-05-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000889302 SCV005261859 likely benign not provided criteria provided, single submitter not provided
Clinical Genetics, Academic Medical Center RCV001700497 SCV001925844 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000889302 SCV001974679 likely benign not provided no assertion criteria provided clinical testing

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