List of variants reported as pathogenic for retinal disorder by Service de Génétique Moléculaire, Hôpital Robert Debré

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004523.4(KIF11):c.2300_2301del (p.Phe767fs)	rs730882121
NM_004523.4(KIF11):c.2922G>A (p.Pro974=)
NM_004523.4(KIF11):c.308+1G>A

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