ClinVar Miner

Submissions for variant NM_001376.5(DYNC1H1):c.6406-4G>A (rs374602014)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000475884 SCV000559759 likely benign not provided 2016-08-11 criteria provided, single submitter clinical testing
Genesis Genome Database RCV000856947 SCV000999511 uncertain significance Charcot-Marie-Tooth disease type 4 2019-08-14 no assertion criteria provided research

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