ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.1698+13C>T (rs80338938)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV001176130 SCV001339997 uncertain significance Cardiomyopathy 2019-11-20 criteria provided, single submitter clinical testing
Epithelial Biology; Institute of Medical Biology, Singapore RCV000057045 SCV000088158 not provided not provided no assertion provided not provided
Inherited Neuropathy Consortium RCV000790249 SCV000929647 uncertain significance Charcot-Marie-Tooth disease no assertion criteria provided literature only

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