ClinVar Miner

Submissions for variant NM_000064.4(C3):c.1686+48TC[8]

dbSNP: rs112132860
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001554508 SCV001775760 benign Complement component 3 deficiency 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001554509 SCV001775761 benign Age related macular degeneration 9 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001595110 SCV001829980 benign not provided 2021-06-18 criteria provided, single submitter clinical testing

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