ClinVar Miner

Submissions for variant NM_001303256.3(MORC2):c.1033G>A (p.Glu345Lys) (rs750686775)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genesis Genome Database RCV000857120 SCV000999698 uncertain significance Charcot-Marie-Tooth disease 2019-08-14 no assertion criteria provided research
Genesis Genome Database RCV000857121 SCV000999699 uncertain significance Charcot-Marie-Tooth disease, type I 2019-08-14 no assertion criteria provided research

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