List of variants in gene BRIP1 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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_032043.3(BRIP1):c.2637A>G (p.Glu879=)	rs4986765	0.74166
NM_032043.3(BRIP1):c.2755T>C (p.Ser919Pro)	rs4986764	0.61453
NM_032043.3(BRIP1):c.3411T>C (p.Tyr1137=)	rs4986763	0.60694
NM_032043.3(BRIP1):c.577G>A (p.Val193Ile)	rs4988346	0.00305
NM_032043.3(BRIP1):c.584T>C (p.Leu195Pro)	rs4988347	0.00197
NM_032043.3(BRIP1):c.2937A>G (p.Lys979=)	rs75091137	0.00194
NM_032043.3(BRIP1):c.2286T>C (p.Arg762=)	rs61754141	0.00173
NM_032043.3(BRIP1):c.2061G>C (p.Val687=)	rs112414873	0.00153
NM_032043.3(BRIP1):c.2257+19A>C	rs77851913	0.00079
NM_032043.3(BRIP1):c.918+15T>A	rs117820198	0.00078
NM_032043.3(BRIP1):c.297C>T (p.Asp99=)	rs201617644	0.00004

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