ClinVar Miner

Submissions for variant NM_033068.3(ACP4):c.419C>T (p.Pro140Leu)

dbSNP: rs1371134137
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dental Genetics Laboratory, Seoul National University School of Dentistry RCV001645019 SCV001519086 uncertain significance Amelogenesis imperfecta 2021-02-03 no assertion criteria provided clinical testing

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