"University of Washington Department of Laboratory Medicine, Universit - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 223606	NM_032043.3(BRIP1):c.628-7337T>C	BRIP1, LOC110120932	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 223612	NM_032043.3(BRIP1):c.628-7464C>T	BRIP1, LOC110120932	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 223609	NM_032043.3(BRIP1):c.628-7560C>T	BRIP1, LOC110120932	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 223614	NM_032043.3(BRIP1):c.628-7768T>G	BRIP1, LOC110120932	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign

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