ClinVar Miner

Submissions for variant NM_002292.4(LAMB2):c.4774C>T (p.Arg1592Trp) (rs61729458)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000251444 SCV000308810 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000350028 SCV000445257 likely benign Pierson syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000407807 SCV000445258 likely benign Nephrotic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000712179 SCV000651560 benign not provided 2019-03-05 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000712179 SCV000842609 benign not provided 2018-04-18 criteria provided, single submitter clinical testing

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