List of variants in gene CRYGS 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_017541.4(CRYGS):c.24T>A (p.Ile8=)	rs113031838	0.00359
NM_017541.4(CRYGS):c.294C>A (p.Ile98=)	rs140421841	0.00198
NM_017541.4(CRYGS):c.306G>A (p.Gly102=)	rs114186269	0.00176
NM_017541.4(CRYGS):c.39C>A (p.Asp13Glu)	rs147971015	0.00032
NM_017541.4(CRYGS):c.77A>G (p.Asp26Gly)	rs143507827	0.00018

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