ClinVar Miner

Submissions for variant NM_000064.4(C3):c.2048-14_2048-13del

dbSNP: rs140718871
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000334669 SCV000415038 benign C3 deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000396795 SCV000415039 benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000295260 SCV000415040 benign Atypical hemolytic-uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001522900 SCV001732528 benign not provided 2024-01-29 criteria provided, single submitter clinical testing

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