List of variants reported as uncertain significance for cataract 20 multiple types

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_017541.4(CRYGS):c.215G>A (p.Arg72His)	rs144812537	0.00026
NM_017541.4(CRYGS):c.299A>C (p.Glu100Ala)	rs375632598	0.00004
NM_017541.4(CRYGS):c.236G>A (p.Arg79His)	rs764969189	0.00003
NM_017541.4(CRYGS):c.62A>G (p.Tyr21Cys)	rs1035614113	0.00001
NM_017541.4(CRYGS):c.107G>A (p.Arg36His)
NM_017541.4(CRYGS):c.139T>C (p.Trp47Arg)
NM_017541.4(CRYGS):c.21+6T>C
NM_017541.4(CRYGS):c.224G>A (p.Gly75Asp)	rs761628147
NM_017541.4(CRYGS):c.247T>C (p.Cys83Arg)	rs1714002505
NM_017541.4(CRYGS):c.248G>A (p.Cys83Tyr)	rs1714002434
NM_017541.4(CRYGS):c.253G>A (p.Ala85Thr)	rs1553846926
NM_017541.4(CRYGS):c.269G>C (p.Ser90Thr)	rs1275239379
NM_017541.4(CRYGS):c.32A>G (p.Tyr11Cys)	rs143424000
NM_017541.4(CRYGS):c.421G>T (p.Glu141Ter)
NM_017541.4(CRYGS):c.436C>T (p.Arg146Cys)
NM_017541.4(CRYGS):c.450C>A (p.Tyr150Ter)
NM_017541.4(CRYGS):c.502C>T (p.Pro168Ser)

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