List of variants in gene CRBN reported 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
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_016302.4(CRBN):c.175-9T>C	rs1669321	0.89132
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.377+13A>C	rs115124101	0.01134
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.634C>G (p.Pro212Ala)	rs141771026	0.00017
NM_016302.4(CRBN):c.654A>G (p.Gln218=)	rs373145132	0.00013
NM_016302.4(CRBN):c.16G>C (p.Asp6His)	rs756440147	0.00010
NM_016302.4(CRBN):c.20A>G (p.Gln7Arg)	rs192011911	0.00009
NM_016302.4(CRBN):c.937G>C (p.Asp313His)	rs142337178	0.00009
NM_016302.4(CRBN):c.584C>T (p.Ser195Phe)	rs1448818496	0.00001
NM_016302.4(CRBN):c.7G>C (p.Gly3Arg)	rs757719993	0.00001
NM_016302.4(CRBN):c.286A>G (p.Thr96Ala)	rs797045481
NM_016302.4(CRBN):c.34C>T (p.His12Tyr)	rs797045482
NM_016302.4(CRBN):c.480T>C (p.Ile160=)	rs2126067673
NM_016302.4(CRBN):c.57_65del (p.Leu20_Pro22del)	rs1553563717

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