ClinVar Miner

Submissions for variant NM_000064.4(C3):c.4120+8G>T

dbSNP: rs886054652
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000284971 SCV000414957 uncertain significance C3 deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000340071 SCV000414958 uncertain significance Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000400915 SCV000414959 uncertain significance Atypical hemolytic-uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing

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