"Department of Molecular Diagnostics, Institute of Oncology Ljubljana" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 91136	NM_000251.3(MSH2):c.561_569del (p.Glu188_Leu190del)	MSH2	Deletion (inframe_deletion)	Lynch syndrome	GPathogenic
Select item 91222	NM_000251.3(MSH2):c.811_814del (p.Ser271fs)	MSH2 (S205fs)	Deletion (frameshift variant)	Lynch syndrome	GPathogenic
Select item 617772	NM_000251.3(MSH2):c.942+1del	MSH2	Deletion (splice donor variant +1 more)	Lynch syndrome +1 more	GLikely pathogenic
Select item 617771	NM_000251.3(MSH2):c.1015C>T (p.Gln339Ter)	MSH2 (Q339* +1 more)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic/Likely pathogenic
Select item 483664	NM_000251.3(MSH2):c.1661G>A (p.Ser554Asn)	MSH2 (S554N +1 more)	Single nucleotide variant (missense variant)	Lynch syndrome 1 +4 more	GPathogenic/Likely pathogenic
Select item 36569	NM_000251.3(MSH2):c.1705_1706del (p.Glu569fs)	MSH2 (E503fs)	Deletion (frameshift variant)	Lynch syndrome	GPathogenic
Select item 1012207	NM_000251.3(MSH2):c.1763_1764del (p.Tyr588fs)	MSH2 (Y522fs +1 more)	Deletion (frameshift variant)	Lynch syndrome 1	GLikely pathogenic

ClinVar