List of variants reported as likely benign for eye degenerative disorder by Service de Génétique Moléculaire, Hôpital Robert Debré

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001376.5(DYNC1H1):c.7203A>C (p.Lys2401Asn)	rs150888094	0.00032
NM_001376.5(DYNC1H1):c.13651G>A (p.Ala4551Thr)	rs145366078	0.00003
NM_001376.5(DYNC1H1):c.11696C>T (p.Pro3899Leu)
NM_001376.5(DYNC1H1):c.5960A>G (p.Asn1987Ser)
NM_001376.5(DYNC1H1):c.9382G>T (p.Val3128Phe)

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