"Narod's Lab, University of Toronto"[submitter] AND "MLH1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 68482	NM_000249.4(MLH1):c.207+12C>T	MLH1	Single nucleotide variant (intron variant)	Hereditary nonpolyposis colorectal neoplasms +2 more	GConflicting classifications of pathogenicity
Select item 68849	NM_000249.4(MLH1):c.307-19A>G	MLH1	Single nucleotide variant (intron variant)	Lynch syndrome	GLikely benign
Select item 68850	NM_000249.4(MLH1):c.380+16C>G	MLH1	Single nucleotide variant (intron variant)	Hereditary nonpolyposis colorectal neoplasms +1 more	GLikely benign
Select item 68851	NM_000249.4(MLH1):c.545+19G>T	MLH1	Single nucleotide variant (intron variant)	Hereditary nonpolyposis colorectal neoplasms +4 more	GConflicting classifications of pathogenicity
Select item 36554	NM_000249.4(MLH1):c.545+20A>T	MLH1	Single nucleotide variant (intron variant)	not specified +5 more	GBenign
Select item 36555	NM_000249.4(MLH1):c.588+11G>C	MLH1	Single nucleotide variant (intron variant)	Lynch syndrome 1	GBenign

ClinVar