List of variants in gene MLH1 reported as benign by Mendelics

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000249.4(MLH1):c.1039-35A>T	rs867680022	0.02046
NM_000249.4(MLH1):c.1963A>G (p.Ile655Val)	rs55907433	0.00297
NM_000249.4(MLH1):c.1321G>A (p.Ala441Thr)	rs63750365	0.00034
NM_000249.4(MLH1):c.2066A>G (p.Gln689Arg)	rs63750702	0.00022
NM_000249.4(MLH1):c.2101C>A (p.Gln701Lys)	rs63750114	0.00016
NM_000249.4(MLH1):c.65G>C (p.Gly22Ala)	rs41295280	0.00016
NM_000249.4(MLH1):c.803A>G (p.Glu268Gly)	rs63750650	0.00014
NM_000249.4(MLH1):c.1742C>T (p.Pro581Leu)	rs63751684	0.00008
NM_000249.4(MLH1):c.1392T>C (p.Pro464=)	rs63750201	0.00005
NM_000249.4(MLH1):c.438A>G (p.Gln146=)	rs377279035	0.00005
NM_000249.4(MLH1):c.845C>G (p.Ala282Gly)	rs63750360	0.00001
NM_000249.3(MLH1):c.-107C>G	rs587778886
NM_000249.4(MLH1):c.1039-31_1039-26del	rs1178900468
NM_000249.4(MLH1):c.1853A>C (p.Lys618Thr)	rs63750449
NM_000249.4(MLH1):c.1989+11_1989+12del	rs2125991370

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