List of variants in gene combination CRYGB, 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_005210.4(CRYGB):c.331A>C (p.Ile111Leu)	rs796287	0.69716
NM_005210.4(CRYGB):c.192T>C (p.Pro64=)	rs2854723	0.48090
NM_005210.4(CRYGB):c.175C>T (p.Arg59Trp)	rs76323117	0.00746
NM_005210.4(CRYGB):c.312A>G (p.Ser104=)	rs200750137	0.00001
NM_005210.4(CRYGB):c.513C>T (p.Val171=)	rs541388467	0.00001
NC_000002.12:g.208146167G>A	rs2289917
NM_005210.4(CRYGB):c.10-38del	rs3214759

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