ClinVar Miner

Submissions for variant NM_182758.4(WDR72):c.3149-30CT[13]

dbSNP: rs57737580
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000397887 SCV000393084 likely benign Amelogenesis Imperfecta, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494992 SCV002799894 likely benign Amelogenesis imperfecta hypomaturation type 2A3 2021-09-12 criteria provided, single submitter clinical testing

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