ClinVar Miner

Submissions for variant NM_000651.6(CR1):c.5811-11C>A

gnomAD frequency: 0.00628  dbSNP: rs115988205
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000514722 SCV000610604 likely benign not provided 2017-06-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002490872 SCV002808885 likely benign KNOPS BLOOD GROUP SYSTEM; Malaria, susceptibility to 2022-04-08 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000514722 SCV005261186 likely benign not provided criteria provided, single submitter not provided

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