ClinVar Miner

Submissions for variant NM_000426.3(LAMA2):c.7965C>A (p.Ile2655=) (rs141101234)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000596361 SCV000700455 uncertain significance not provided 2017-03-29 criteria provided, single submitter clinical testing
Invitae RCV000534174 SCV000658769 benign Laminin alpha 2-related dystrophy 2017-11-18 criteria provided, single submitter clinical testing

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