ClinVar Miner

Submissions for variant NM_001710.5(CFB):c.672C>T (p.Tyr224=) (rs4151670)

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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 RCV000326038 SCV000462025 likely benign Atypical hemolytic uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000332230 SCV000462026 likely benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000270236 SCV000484225 likely benign Complement component 2 deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000332230 SCV000484226 likely benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing

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