ClinVar Miner

Submissions for variant NM_198173.3(GRHL3):c.1285+2del (rs886037770)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ludwig Lab, Institute of Human Genetics, University Hospital Bonn RCV000240817 SCV000258553 pathogenic nonsyndromic cleft palate 2015-12-01 criteria provided, single submitter research

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