List of variants reported as likely pathogenic for corneal disorder by Juha Muilu Group; Institute for Molecular Medicine Finland (FIMM)

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_007035.4(KERA):c.835C>T (p.Arg279Ter)	rs386833986	0.00004
NM_007035.4(KERA):c.391A>G (p.Asn131Asp)	rs386833985	0.00001
NM_007035.4(KERA):c.1026del (p.Cys343fs)	rs386833984

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