List of variants in gene CRBN reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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_016302.4(CRBN):c.88G>A (p.Glu30Lys)	rs78564552	0.00266
NM_016302.4(CRBN):c.255A>G (p.Pro85=)
NM_016302.4(CRBN):c.279C>A (p.Pro93=)	rs773279779
NM_016302.4(CRBN):c.411A>C (p.Thr137=)
NM_016302.4(CRBN):c.576A>C (p.Ser192=)

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