ClinVar Miner

Submissions for variant NM_005676.5(RBM10):c.1249-1G>A

dbSNP: rs1556778986
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000503825 SCV000596730 pathogenic TARP syndrome 2016-06-24 criteria provided, single submitter clinical testing

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