ClinVar Miner

Submissions for variant NM_000186.3(CFH):c.1949G>T (p.Gly650Val) (rs143237092)

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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 RCV000289073 SCV000352420 likely benign Atypical hemolytic uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000344087 SCV000352421 likely benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000403698 SCV000352422 likely benign Mesangiocapillary glomerulonephritis, type II 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000309119 SCV000352423 likely benign Basal laminar drusen 2016-06-14 criteria provided, single submitter clinical testing

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