ClinVar Miner

Submissions for variant NM_173602.3(DIP2B):c.998G>C (p.Cys333Ser)

dbSNP: rs1006854230
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Total submissions: 1
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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 RCV000425066 SCV000510842 uncertain significance not provided 2017-01-09 criteria provided, single submitter clinical testing Converted during submission to Uncertain significance.

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