C3150547[trait identifier] AND "MGZ Medical Genetics Center"[submitter - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 126681	NM_024675.4(PALB2):c.2773G>C (p.Val925Leu)	PALB2 (V925L)	Single nucleotide variant (missense variant)	Familial cancer of breast +5 more	GUncertain significance
Select item 136132	NM_024675.4(PALB2):c.2167_2168del (p.Met723fs)	PALB2	Deletion (frameshift variant)	Fanconi anemia complementation group N +8 more	GPathogenic
Select item 141972	NM_024675.4(PALB2):c.1748T>G (p.Leu583Trp)	PALB2 (L583W)	Single nucleotide variant (missense variant)	Familial cancer of breast	GUncertain significance FDA Recognized database
Select item 126768	NM_024675.4(PALB2):c.757_758del (p.Leu253fs)	PALB2 (L253fs)	Microsatellite (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 1 +6 more	GPathogenic
Select item 126757	NM_024675.4(PALB2):c.509_510del (p.Arg170fs)	PALB2	Deletion (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 1 +11 more	GPathogenic
Select item 126623	NM_024675.4(PALB2):c.172_175del (p.Gln60fs)	PALB2 (Q60fs)	Microsatellite (frameshift variant)	Hereditary breast ovarian cancer syndrome +5 more	GPathogenic/Likely pathogenic
Select item 1350833	NM_024675.4(PALB2):c.86_108+12dup	PALB2	Duplication (splice donor variant)	Pancreatic cancer, susceptibility to, 3 +2 more	GUncertain significance
Select item 220371	NM_024675.4(PALB2):c.93dup (p.Leu32fs)	PALB2 (L32fs)	Duplication	Familial cancer of breast +4 more	GPathogenic/Likely pathogenic

ClinVar