List of variants in gene CRBN reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_016302.4(CRBN):c.735T>C (p.Tyr245=)	rs17027638	0.05605
NM_016302.4(CRBN):c.219C>T (p.His73=)	rs1045309	0.01725
NM_016302.4(CRBN):c.175-5T>A	rs151039737	0.01132
NM_016302.4(CRBN):c.88G>A (p.Glu30Lys)	rs78564552	0.00266
NM_016302.4(CRBN):c.564T>C (p.Cys188=)	rs150595840	0.00053
NM_016302.4(CRBN):c.480T>C (p.Ile160=)	rs2126067673

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