ClinVar Miner

Submissions for variant NM_001710.5(CFB):c.1137C>T (p.Arg379=) (rs45600936)

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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 RCV000282122 SCV000462039 likely benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000362438 SCV000462040 likely benign Atypical hemolytic uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000282122 SCV000484231 likely benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000334269 SCV000484232 likely benign Complement component 2 deficiency 2016-06-14 criteria provided, single submitter clinical testing

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