ClinVar Miner

Submissions for variant NM_001710.5(CFB):c.1778+9G>A (rs188688680)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000266451 SCV000462061 likely benign Atypical hemolytic uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000324029 SCV000462062 likely benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing

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