List of variants in gene BRD4 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001379291.1(BRD4):c.285+44G>T	rs34855805	0.19620
NM_001379291.1(BRD4):c.285+110G>A	rs2240304	0.16363
NM_001379291.1(BRD4):c.2865A>C (p.Pro955=)	rs775889378	0.05892
NM_001379291.1(BRD4):c.1342-108C>T	rs73508410	0.03480
NM_001379291.1(BRD4):c.1950C>T (p.Asp650=)	rs17707730	0.02727
NM_001379291.1(BRD4):c.1342-144C>T	rs80227750	0.01865
NM_001379291.1(BRD4):c.3446-34G>A	rs60057301	0.01559
NM_001379291.1(BRD4):c.2047+89_2047+90dup	rs71333363
NM_001379291.1(BRD4):c.2047+89dup	rs71333363
NM_001379291.1(BRD4):c.286-206dup	rs112184222
NM_001379291.1(BRD4):c.424-76_424-73del	rs139141985

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