ClinVar Miner

Submissions for variant NM_000064.4(C3):c.3671G>A (p.Gly1224Asp) (rs11569534)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Blueprint Genetics RCV000788906 SCV000928197 uncertain significance not provided 2019-01-29 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000338521 SCV000414975 likely benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000396966 SCV000414976 likely benign C3 deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000279638 SCV000414977 likely benign Atypical hemolytic uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing

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