ClinVar Miner

Submissions for variant NM_000186.3(CFH):c.3176T>C (p.Ile1059Thr) (rs35343172)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000363925 SCV000343684 benign not specified 2016-08-11 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000270018 SCV000352514 likely benign Atypical hemolytic uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000327390 SCV000352515 likely benign Basal laminar drusen 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000384228 SCV000352516 likely benign Mesangiocapillary glomerulonephritis, type II 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000292141 SCV000352517 likely benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing

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