ClinVar Miner

List of variants reported as likely pathogenic for Congenital primary aphakia by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_012186.3(FOXE3):c.244A>G (p.Met82Val)	rs746531116	0.00005
NM_012186.3(FOXE3):c.632C>A (p.Ser211Ter)	rs1035206433	0.00002

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