List of variants in gene BRIP1 reported as uncertain significance by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.139C>G (p.Pro47Ala)	rs28903098	0.00024
NM_032043.3(BRIP1):c.1984G>A (p.Ala662Thr)	rs571340013	0.00001
NM_032043.3(BRIP1):c.1871C>T (p.Ser624Leu)	rs587781321
NM_032043.3(BRIP1):c.2319T>A (p.Asp773Glu)	rs1555590447

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