"Sema4, Sema4"[submitter] AND "LOC110485084"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1692984	NM_007294.4(BRCA1):c.81-3898C>G	BRCA1, LOC110485084	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1692985	NM_007294.4(BRCA1):c.81-4038G>A	BRCA1, LOC110485084 +1 more	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1692980	NM_007294.4(BRCA1):c.80+4068T>A	BRCA1, LOC110485084 +1 more	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 264781	NM_007294.4(BRCA1):c.80+4068T>C	BRCA1, LOC110485084 +1 more	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 1	GBenign
Select item 1692979	NM_007294.4(BRCA1):c.80+4041C>T	BRCA1, LOC110485084 +1 more	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1692978	NM_007294.4(BRCA1):c.80+4041C>G	BRCA1, LOC110485084 +1 more	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GBenign

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