List of variants in gene CRYBB3 reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_004076.5(CRYBB3):c.-20-13T>C	rs2269672	0.60394
NM_004076.5(CRYBB3):c.337C>G (p.His113Asp)	rs9608378	0.58489
NM_004076.5(CRYBB3):c.75+273_75+274insAT	rs3064261	0.49483
NM_004076.5(CRYBB3):c.471-230A>G	rs2252880	0.42658
NM_004076.5(CRYBB3):c.471-224G>A	rs2283810	0.18754
NM_004076.5(CRYBB3):c.75+188C>T	rs2027889	0.07859
NM_004076.5(CRYBB3):c.471-6C>T	rs13055430	0.06273
NM_004076.5(CRYBB3):c.470+136C>T	rs113538872	0.04774
NM_004076.5(CRYBB3):c.314G>A (p.Arg105Gln)	rs17670506	0.04364
NM_004076.5(CRYBB3):c.327+130A>G	rs16979730	0.03536
NM_004076.5(CRYBB3):c.328-111G>T	rs150956294	0.02901
NM_004076.5(CRYBB3):c.328-301C>A	rs115234626	0.01467
NM_004076.5(CRYBB3):c.567G>A (p.Pro189=)	rs144842183	0.00997
NM_004076.5(CRYBB3):c.470+160C>T	rs56398932
NM_004076.5(CRYBB3):c.471-306G>A	rs2252878

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