ClinVar Miner

Submissions for variant NM_000186.3(CFH):c.2808G>T (p.Glu936Asp) (rs1065489)

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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 RCV000406400 SCV000352465 benign Atypical hemolytic uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000307823 SCV000352466 benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000362551 SCV000352467 benign Mesangiocapillary glomerulonephritis, type II 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000272281 SCV000352468 benign Basal laminar drusen 2016-06-14 criteria provided, single submitter clinical testing

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