List of variants in gene CRYBB3 reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004076.5(CRYBB3):c.471-6C>T	rs13055430	0.06273
NM_004076.5(CRYBB3):c.314G>A (p.Arg105Gln)	rs17670506	0.04364
NM_004076.5(CRYBB3):c.328-73C>T	rs117311393	0.01399
NM_004076.5(CRYBB3):c.567G>A (p.Pro189=)	rs144842183	0.00997
NM_004076.5(CRYBB3):c.125C>T (p.Ser42Leu)	rs145770544	0.00192

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