ClinVar Miner

Submissions for variant NM_017565.4(FAM20A):c.1219+3_1219+6del

dbSNP: rs2086254952
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Medical Molecular Genetics, National Research Centre RCV001093647 SCV001147025 likely pathogenic Amelogenesis imperfecta type 1G 2019-09-01 criteria provided, single submitter clinical testing

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