C2676676[trait identifier] AND "MVZ Praenatalmedizin und Genetik Nuern - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 433193	NM_007294.4(BRCA1):c.3590del (p.His1197fs)	BRCA1, LOC126862571 (H1197fs +21 more)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 54890	NM_007294.4(BRCA1):c.3454G>A (p.Asp1152Asn)	BRCA1, LOC126862571 (D1152N +21 more)	Single nucleotide variant (intron variant +1 more)	Familial cancer of breast +5 more	GConflicting classifications of pathogenicity
Select item 54113	NM_007294.4(BRCA1):c.1065G>A (p.Lys355=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 599300	NM_007294.4(BRCA1):c.343_344del (p.Ser114_Pro115insTer)	BRCA1	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 54844	NM_007294.4(BRCA1):c.332A>C (p.Glu111Ala)	BRCA1 (E111A +5 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 868146	NM_007294.4(BRCA1):c.109A>G (p.Thr37Ala)	BRCA1 (T37A)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely pathogenic

ClinVar