ClinVar (all) for Orgtrack (Select 506675) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 221910	NM_133510.4(RAD51B):c.84G>A (p.Gln28=)	RAD51B	Single nucleotide variant (synonymous variant +1 more)	Hereditary breast ovarian cancer syndrome +1 more	GLikely pathogenic
Select item 216577	NM_004329.3(BMPR1A):c.1274A>T (p.Tyr425Phe)	BMPR1A (Y425F)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 127891	NM_002878.4(RAD51D):c.493C>T (p.Arg165Trp)	RAD51D, RAD51L3-RFFL (R165W +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +4 more	GUncertain significance
Select item 127446	NM_000051.4(ATM):c.7475T>G (p.Leu2492Arg)	ATM, C11orf65 (L2492R)	Single nucleotide variant (missense variant +1 more)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 13936	NM_020975.6(RET):c.2372A>T (p.Tyr791Phe)	RET (Y791F +17 more)	Single nucleotide variant (missense variant)	not provided +9 more	GBenign/Likely benign
Select item 4736	NM_032043.3(BRIP1):c.139C>G (p.Pro47Ala)	BRIP1 (P47A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +7 more	GConflicting classifications of pathogenicity

ClinVar