ClinVar Miner

Submissions for variant NM_000381.4(MID1):c.420C>G (p.Ser140=)

gnomAD frequency: 0.00004  dbSNP: rs201845920
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000195165 SCV000248046 uncertain significance not specified 2014-09-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003718132 SCV004508932 benign not provided 2024-01-25 criteria provided, single submitter clinical testing

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