"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "LOC1067217 - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1166054	NM_000059.4(BRCA2):c.-296C>T	BRCA2, LOC106721785	Single nucleotide variant	Hereditary breast ovarian cancer syndrome +3 more	GBenign/Likely benign
Select item 882070	NM_000059.3(BRCA2):c.-220G>T	BRCA2, LOC106721785	Single nucleotide variant	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 264955	NM_000059.4(BRCA2):c.-162G>A	BRCA2, LOC106721785	Single nucleotide variant (5 prime UTR variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 807001	NM_000059.4(BRCA2):c.-57A>G	BRCA2, LOC106721785	Single nucleotide variant (5 prime UTR variant)	Hereditary breast ovarian cancer syndrome +1 more	GUncertain significance

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