ClinVar Miner

Submissions for variant NM_000064.4(C3):c.1119+15G>A (rs114252882)

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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 RCV000299557 SCV000415086 likely benign Atypical hemolytic uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000368315 SCV000415087 likely benign C3 deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000277555 SCV000415088 likely benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing

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