List of variants in gene BRIP1 reported as pathogenic by Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center

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_032043.3(BRIP1):c.2392C>T (p.Arg798Ter)	rs137852986	0.00010
NM_032043.3(BRIP1):c.1871C>A (p.Ser624Ter)	rs587781321	0.00006
NM_032043.3(BRIP1):c.2108delinsTCC (p.Lys703fs)	rs786203384
NM_032043.3(BRIP1):c.2255_2256del (p.Lys752fs)	rs730881649
NM_032043.3(BRIP1):c.2990_2993del (p.Thr997fs)	rs771028677

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