ClinVar Miner

Submissions for variant NM_000186.3(CFH):c.275C>T (p.Pro92Leu) (rs886045743)

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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 RCV000406315 SCV000352356 uncertain significance Basal laminar drusen 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000284800 SCV000352357 uncertain significance Atypical hemolytic uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000346805 SCV000352358 uncertain significance Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000402549 SCV000352359 uncertain significance Mesangiocapillary glomerulonephritis, type II 2016-06-14 criteria provided, single submitter clinical testing

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