ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.357-739T>G

gnomAD frequency: 0.18886  dbSNP: rs513043
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biesecker Lab/Clinical Genomics Section, National Institutes of Health RCV000172758 SCV000051561 benign not specified 2013-06-24 criteria provided, single submitter research
Mendelics RCV000986428 SCV001135428 benign Hutchinson-Gilford syndrome 2019-05-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004713393 SCV005282272 benign not provided criteria provided, single submitter not provided

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