ClinVar Miner

Submissions for variant NM_002292.4(LAMB2):c.2922G>C (p.Gly974=) (rs145465720)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000304855 SCV000445299 uncertain significance Pierson syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000341133 SCV000445300 uncertain significance Nephrotic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000537395 SCV000651536 likely benign not provided 2018-09-19 criteria provided, single submitter clinical testing

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