ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.1535T>C (p.Leu512Pro) (rs57877560)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Epithelial Biology; Institute of Medical Biology, Singapore RCV000057319 SCV000088432 not provided not provided no assertion provided not provided
Inherited Neuropathy Consortium RCV000789669 SCV000929044 uncertain significance Hereditary liability to pressure palsies no assertion criteria provided literature only

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