ClinVar Miner

Submissions for variant NM_000064.4(C3):c.1836G>A (p.Thr612=) (rs2230205)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000358505 SCV000415050 benign C3 deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000266157 SCV000415051 benign Atypical hemolytic uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000318975 SCV000415052 benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing

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