ClinVar Miner

Submissions for variant NM_002292.4(LAMB2):c.306C>T (p.Asn102=) (rs79448908)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000242586 SCV000308805 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000399816 SCV000445341 likely benign Pierson syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000299339 SCV000445342 likely benign Nephrotic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000550042 SCV000651537 benign Pierson syndrome; Nephrotic syndrome, type 5, with or without ocular abnormalities 2017-08-08 criteria provided, single submitter clinical testing

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