ClinVar Miner

Submissions for variant NM_025214.3(CCDC68):c.775dup (p.Ser259fs)

dbSNP: rs2044011378
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department Of Translational Genomics (developmental Genetics Section), King Faisal Specialist Hospital & Research Centre RCV001250896 SCV001161797 likely pathogenic Recurrent spontaneous abortion 2020-01-27 no assertion criteria provided research

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