C1833477[trait identifier] AND "Human Genetics Bochum, Ruhr University - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2583145	NM_000179.3(MSH6):c.691del (p.Val231fs)	MSH6 (V101fs +7 more)	Deletion (frameshift variant +3 more)	Lynch syndrome 5	GLikely pathogenic
Select item 89174	NM_000179.3(MSH6):c.1135_1139del (p.Arg378_Arg379insTer)	MSH6	Microsatellite (nonsense)	Lynch syndrome	GPathogenic
Select item 89197	NM_000179.3(MSH6):c.1483C>T (p.Arg495Ter)	MSH6 (R495* +2 more)	Single nucleotide variant (nonsense)	Lynch syndrome	GPathogenic
Select item 2583146	NM_000179.3(MSH6):c.2977del (p.Glu993fs)	MSH6 (E1025fs +9 more)	Deletion (frameshift variant +2 more)	Lynch syndrome 5	GLikely pathogenic
Select item 428320	NM_000179.3(MSH6):c.3514_3515insAA (p.Arg1172fs)	MSH6 (R1172fs +2 more)	Insertion (frameshift variant)	Familial prostate cancer +3 more	GPathogenic/Likely pathogenic
Select item 2583152	NM_000179.3(MSH6):c.3955_3974dup (p.Met1326fs)	MSH6 (M1024fs +14 more)	Duplication (frameshift variant +3 more)	Lynch syndrome 5	GLikely pathogenic
Select item 42472	NM_000179.3(MSH6):c.3991C>T (p.Arg1331Ter)	MSH6 (R1331* +2 more)	Single nucleotide variant (nonsense)	Lynch syndrome	GPathogenic

ClinVar