List of variants reported as pathogenic for cataract 18

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_024513.4(FYCO1):c.4271G>A (p.Arg1424Gln)	rs140159323	0.00019
NM_024513.4(FYCO1):c.2206C>T (p.Gln736Ter)	rs387906964	0.00002
NM_024513.4(FYCO1):c.1411C>T (p.Arg471Ter)	rs768945306	0.00001
NM_024513.4(FYCO1):c.3150+1G>T	rs766522434	0.00001
NM_024513.4(FYCO1):c.1045C>T (p.Gln349Ter)	rs387906963
NM_024513.4(FYCO1):c.1546C>T (p.Gln516Ter)	rs387906966
NM_024513.4(FYCO1):c.2345del (p.Gln782fs)
NM_024513.4(FYCO1):c.2505del (p.Ala836fs)	rs1575369255
NM_024513.4(FYCO1):c.265_267delinsTGA (p.Arg89Ter)
NM_024513.4(FYCO1):c.3161del (p.Ala1054fs)	rs2125846016
NM_024513.4(FYCO1):c.3322A>T (p.Lys1108Ter)	rs73830668
NM_024513.4(FYCO1):c.3327_3328del (p.Cys1110fs)	rs747093432
NM_024513.4(FYCO1):c.3858_3862dup (p.Leu1288fs)	rs1240503246
NM_024513.4(FYCO1):c.3861del (p.Glu1287fs)	rs777269054
NM_024513.4(FYCO1):c.4127T>C (p.Leu1376Pro)	rs387906965
NM_024513.4(FYCO1):c.524G>A (p.Trp175Ter)	rs2125859216
NM_024513.4(FYCO1):c.528_529insGGCAAAGT (p.Thr177fs)	rs2125859204
NM_024513.4(FYCO1):c.575G>A (p.Trp192Ter)	rs200679450

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