ClinVar Miner

Submissions for variant NM_012064.4(MIP):c.508dup (p.Leu170fs)

dbSNP: rs1057519616
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Medical Genetic Institute of Henan Province, Henan Provincial People’s Hospital RCV000420543 SCV000292029 pathogenic Cataract 15 multiple types 2015-12-16 no assertion criteria provided clinical testing

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