List of variants in gene BRIP1 reported as likely benign by Genome Diagnostics Laboratory, Amsterdam University Medical 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.577G>A (p.Val193Ile)	rs4988346	0.00297
NM_032043.3(BRIP1):c.2097+7G>A	rs4988352	0.00271
NM_032043.3(BRIP1):c.584T>C (p.Leu195Pro)	rs4988347	0.00197
NM_032043.3(BRIP1):c.618G>T (p.Ser206=)	rs367614726

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