ClinVar Miner

Submissions for variant NM_001303256.3(MORC2):c.598A>G (p.Ile200Val)

gnomAD frequency: 0.00001  dbSNP: rs765371898
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002136071 SCV002458278 likely benign Charcot-Marie-Tooth disease axonal type 2Z 2021-11-06 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003130691 SCV003808896 uncertain significance not provided 2021-11-15 criteria provided, single submitter clinical testing

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