List of variants in gene LIM2 reported as likely benign for cataract

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001161748.2(LIM2):c.175+11C>T	rs73933350	0.00824
NM_001161748.2(LIM2):c.175+83A>G	rs201295572	0.00055
NM_001161748.2(LIM2):c.175+50G>A	rs147625714	0.00029
NM_001161748.2(LIM2):c.369C>T (p.Thr123=)	rs200033512	0.00009
NM_001161748.2(LIM2):c.326-15G>A	rs752385175	0.00006
NM_001161748.2(LIM2):c.-27C>T	rs113926789
NM_001161748.2(LIM2):c.144C>T (p.Gly48=)
NM_001161748.2(LIM2):c.222C>T (p.Cys74=)
NM_001161748.2(LIM2):c.460+13A>T
NM_001161748.2(LIM2):c.461-15C>A

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