List of variants in gene combination CRYGC, LOC100507443 reported as 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_020989.4(CRYGC):c.357C>T (p.Ser119=)	rs61736036	0.01345
NM_020989.4(CRYGC):c.143G>A (p.Arg48His)	rs61751949	0.01047
NM_020989.4(CRYGC):c.123C>T (p.Gly41=)	rs115828074	0.00612
NM_020989.4(CRYGC):c.317G>A (p.Ser106Asn)	rs149859061	0.00366
NM_020989.4(CRYGC):c.10-10T>C	rs199901300	0.00136
NM_020989.4(CRYGC):c.84G>A (p.Pro28=)	rs142890808	0.00034
NM_020989.4(CRYGC):c.120C>T (p.Ser40=)	rs184571576	0.00023
NM_020989.4(CRYGC):c.10-14T>C	rs367944766	0.00022
NM_020989.4(CRYGC):c.364C>T (p.Arg122Cys)	rs368393196	0.00005
NM_020989.4(CRYGC):c.33C>T (p.Ala11=)	rs533923837	0.00004

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