List of variants reported as likely benign for Cataract 30

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_003380.5(VIM):c.542A>C (p.Asp181Ala)	rs149942621	0.00115
NM_003380.5(VIM):c.749A>G (p.Gln250Arg)	rs145152785	0.00104
NM_003380.5(VIM):c.1360-18G>T	rs535331705	0.00042
NM_003380.5(VIM):c.882+7A>C	rs188726419	0.00041
NM_003380.5(VIM):c.987A>G (p.Glu329=)	rs147429387	0.00026
NM_003380.5(VIM):c.624+7A>G	rs376197279	0.00025
NM_003380.5(VIM):c.774G>A (p.Val258=)	rs141519986	0.00025
NM_003380.5(VIM):c.624+17C>G	rs372092479	0.00015
NM_003380.5(VIM):c.384T>C (p.Asn128=)	rs147857896	0.00013
NM_003380.5(VIM):c.1360-17T>G	rs764183925	0.00010
NM_003380.5(VIM):c.1368C>T (p.Asn456=)	rs753533838	0.00005
NM_003380.5(VIM):c.882+20G>A	rs370279416	0.00004
NM_003380.5(VIM):c.1009-8C>A	rs372984113	0.00003
NM_003380.5(VIM):c.1122G>A (p.Glu374=)	rs749331181	0.00003
NM_003380.5(VIM):c.563+15A>C	rs745329934	0.00001
NM_003380.5(VIM):c.423A>G (p.Gln141=)	rs2131679660
NM_003380.5(VIM):c.624+7A>C	rs376197279
NM_003380.5(VIM):c.990G>C (p.Val330=)	rs2493191415

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