ClinVar Miner

Submissions for variant NM_017813.5(BPNT2):c.*5689dup

dbSNP: rs200630025
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000280405 SCV000474224 likely benign Chondrodysplasia 2016-06-14 criteria provided, single submitter clinical testing

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