List of variants reported as likely pathogenic for retinal disorder by Institute of Human Genetics, University of Goettingen

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000390.4(CHM):c.1402del (p.Ser468fs)
NM_003816.3(ADAM9):c.1616del (p.Cys539fs)
NM_004523.4(KIF11):c.376dup (p.Thr126fs)	rs2135901156
NM_015629.4(PRPF31):c.945+2T>G	rs2146437002
NM_133497.4(KCNV2):c.153T>G (p.Tyr51Ter)	rs950492553

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