List of variants in gene MLH1 reported as likely benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000249.4(MLH1):c.1959G>T (p.Leu653=)	rs1800146	0.00913
NM_000249.4(MLH1):c.2146G>A (p.Val716Met)	rs35831931	0.00143
NM_000249.4(MLH1):c.1379A>C (p.Glu460Ala)	rs202038499	0.00007
NM_000249.4(MLH1):c.649C>T (p.Arg217Cys)	rs4986984	0.00007
NM_000249.4(MLH1):c.1104G>A (p.Ser368=)	rs769364808	0.00006
NM_000249.4(MLH1):c.1269G>A (p.Arg423=)	rs373076967	0.00004
NM_000249.4(MLH1):c.303T>G (p.Gly101=)	rs4647220	0.00002
NM_000249.4(MLH1):c.1039-8_1039-7insTA	rs535965616
NM_000249.4(MLH1):c.1039-8_1039-7insTTTTTTTA	rs535965616

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