ClinVar Miner

Submissions for variant NM_000186.3(CFH):c.3004G>C (p.Gly1002Arg) (rs201816520)

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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 RCV000341877 SCV000352481 uncertain significance Basal laminar drusen 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000408202 SCV000352482 uncertain significance Mesangiocapillary glomerulonephritis, type II 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000307054 SCV000352483 uncertain significance Atypical hemolytic uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000347912 SCV000352484 uncertain significance Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing

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