ClinVar Miner

Submissions for variant NM_000186.3(CFH):c.3138C>T (p.Thr1046=) (rs61822181)

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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 RCV000391333 SCV000352502 benign Basal laminar drusen 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000295182 SCV000352503 benign Atypical hemolytic uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000352377 SCV000352504 benign Mesangiocapillary glomerulonephritis, type II 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000404495 SCV000352505 benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing

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