List of variants in gene MLH1 reported as likely benign by Mayo Clinic Laboratories, Mayo Clinic

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000249.4(MLH1):c.2152C>T (p.His718Tyr)	rs2020873	0.02345
NM_000249.4(MLH1):c.1039-29del	rs746933807	0.01004
NM_000249.4(MLH1):c.453+25A>G	rs4647246	0.00414
NM_000249.4(MLH1):c.307-29C>A	rs139620056	0.00398
NM_000249.4(MLH1):c.1963A>G (p.Ile655Val)	rs55907433	0.00297
NM_000249.4(MLH1):c.790+10A>G	rs182733777	0.00188
NM_000249.4(MLH1):c.885-24T>A	rs201594027	0.00164
NM_000249.4(MLH1):c.1039-25T>A	rs764852270	0.00064
NM_000249.4(MLH1):c.1039-24T>A	rs1285179213	0.00048
NM_000249.4(MLH1):c.702G>A (p.Glu234=)	rs35908749	0.00041
NM_000249.4(MLH1):c.198C>T (p.Thr66=)	rs61751642	0.00040
NM_000249.4(MLH1):c.977T>C (p.Val326Ala)	rs63751049	0.00037
NM_000249.4(MLH1):c.843A>C (p.Ala281=)	rs146796765	0.00012
NM_000249.4(MLH1):c.277A>G (p.Ser93Gly)	rs41295282	0.00007
NM_000249.4(MLH1):c.1558+22C>T	rs863225374	0.00002
NM_000249.4(MLH1):c.2091C>T (p.Leu697=)	rs536488280

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