ClinVar Miner

Submissions for variant NM_000186.4(CFH):c.428-3C>T

dbSNP: rs886045744
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000321856 SCV000352372 uncertain significance Mesangiocapillary glomerulonephritis, type II 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000383535 SCV000352373 uncertain significance Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000291509 SCV000352374 uncertain significance Basal laminar drusen 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000343575 SCV000352375 uncertain significance Atypical hemolytic-uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing

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