ClinVar Miner

Submissions for variant NM_001029882.3(AHDC1):c.-971A>G

dbSNP: rs878853068
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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 RCV000224362 SCV000281244 uncertain significance not provided 2015-02-11 criteria provided, single submitter clinical testing Converted during submission to Uncertain significance.

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