ClinVar Miner

Submissions for variant NM_001122681.2(SH3BP2):c.*7167del

dbSNP: rs566926916
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000305224 SCV000449344 uncertain significance Fibrous dysplasia of jaw 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004695793 SCV005189990 uncertain significance not provided criteria provided, single submitter not provided

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