ClinVar Miner

Submissions for variant NM_000064.4(C3):c.3646+98A>G

gnomAD frequency: 0.87336  dbSNP: rs237554
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001554743 SCV001776046 benign Complement component 3 deficiency 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001554744 SCV001776047 benign Age related macular degeneration 9 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001615330 SCV001841045 benign not provided 2018-11-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001615330 SCV005310222 benign not provided criteria provided, single submitter not provided

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