ClinVar Miner

Submissions for variant NM_001710.5(CFB):c.504G>A (p.Pro168=) (rs4151669)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000353755 SCV000462017 likely benign Atypical hemolytic uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000263692 SCV000462018 likely benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000263692 SCV000484221 likely benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000271771 SCV000484222 likely benign Complement component 2 deficiency 2016-06-14 criteria provided, single submitter clinical testing

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