ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.626del (p.Asn209fs)

dbSNP: rs62636507
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Blueprint Genetics RCV000057434 SCV000927415 likely pathogenic not provided 2017-09-28 criteria provided, single submitter clinical testing
Epithelial Biology; Institute of Medical Biology, Singapore RCV000057434 SCV000088548 not provided not provided no assertion provided not provided

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