List of variants in gene BRIP1 reported as benign by Color Diagnostics, LLC DBA Color Health

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: 18

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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.94-18T>G	rs2138005	0.03086
NM_032043.3(BRIP1):c.577G>A (p.Val193Ile)	rs4988346	0.00305
NM_032043.3(BRIP1):c.2937A>G (p.Lys979=)	rs75091137	0.00194
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.195A>G (p.Gln65=)	rs141436143	0.00076
NM_032043.3(BRIP1):c.3378A>C (p.Glu1126Asp)	rs145855459	0.00076
NM_032043.3(BRIP1):c.430G>A (p.Ala144Thr)	rs116952709	0.00055
NM_032043.3(BRIP1):c.317G>A (p.Arg106His)	rs143615668	0.00048
NM_032043.3(BRIP1):c.587A>G (p.Asn196Ser)	rs550707862	0.00017
NM_032043.3(BRIP1):c.3099T>C (p.Pro1033=)	rs202228407	0.00013
NM_032043.3(BRIP1):c.1433A>G (p.His478Arg)	rs45501097	0.00002
NM_032043.3(BRIP1):c.1474-3T>C	rs552752779	0.00001
NM_032043.3(BRIP1):c.1935+5GTT[2]	rs730881641
NM_032043.3(BRIP1):c.380-17del	rs545021924

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