List of variants in gene combination CRYGB, LOC100507443 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_005210.4(CRYGB):c.137A>G (p.Tyr46Cys)	rs370785666	0.00019
NM_005210.4(CRYGB):c.179G>A (p.Arg60His)
NM_005210.4(CRYGB):c.21C>T (p.Tyr7=)
NM_005210.4(CRYGB):c.9+11_9+13delinsAAA	rs386654563

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