ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.1622G>C (p.Arg541Pro)

dbSNP: rs61444459
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000057345 SCV000595611 likely pathogenic not provided 2016-03-15 criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000057345 SCV000707237 pathogenic not provided 2017-03-29 criteria provided, single submitter clinical testing
Epithelial Biology; Institute of Medical Biology, Singapore RCV000057345 SCV000088458 not provided not provided no assertion provided not provided

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