ClinVar Miner

Submissions for variant NM_001303256.3(MORC2):c.2380+1G>A

dbSNP: rs113045177
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000990421 SCV001141404 uncertain significance Charcot-Marie-Tooth disease axonal type 2Z 2019-05-28 criteria provided, single submitter clinical testing

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