ClinVar Miner

Submissions for variant NM_000186.3(CFH):c.1736T>C (p.Val579Ala) (rs201411537)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000317574 SCV000352412 likely benign Atypical hemolytic uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000372197 SCV000352413 likely benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000282381 SCV000352414 likely benign Basal laminar drusen 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000336971 SCV000352415 likely benign Mesangiocapillary glomerulonephritis, type II 2016-06-14 criteria provided, single submitter clinical testing

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