ClinVar Miner

Submissions for variant NM_001024630.4(RUNX2):c.254C>T (p.Ala85Val) (rs372138746)

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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 RCV000435406 SCV000510740 likely benign not provided 2016-10-03 criteria provided, single submitter clinical testing Converted during submission to Likely benign.
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000999874 SCV000886061 benign not specified 2019-05-22 criteria provided, single submitter clinical testing
Invitae RCV000435406 SCV001105852 benign not provided 2017-07-11 criteria provided, single submitter clinical testing

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