List of variants in gene MLH1 reported as benign by Quest Diagnostics Nichols Institute San Juan Capistrano

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_000249.4(MLH1):c.1963A>G (p.Ile655Val)	rs55907433	0.00297
NM_000249.4(MLH1):c.-7C>T	rs104894994	0.00115
NM_000249.4(MLH1):c.-28A>G	rs56198082	0.00110
NM_000249.4(MLH1):c.375A>G (p.Ala125=)	rs1800144	0.00062
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.1321G>A (p.Ala441Thr)	rs63750365	0.00034
NM_000249.4(MLH1):c.487A>C (p.Arg163=)	rs748500860	0.00029
NM_000249.4(MLH1):c.2066A>G (p.Gln689Arg)	rs63750702	0.00022
NM_000249.4(MLH1):c.394G>C (p.Asp132His)	rs28930073	0.00019
NM_000249.4(MLH1):c.2101C>A (p.Gln701Lys)	rs63750114	0.00016
NM_000249.4(MLH1):c.2001C>T (p.Asp667=)	rs63750014	0.00014
NM_000249.4(MLH1):c.803A>G (p.Glu268Gly)	rs63750650	0.00014
NM_000249.4(MLH1):c.1050A>G (p.Pro350=)	rs137937003	0.00012
NM_000249.4(MLH1):c.843A>C (p.Ala281=)	rs146796765	0.00012
NM_000249.4(MLH1):c.1808C>G (p.Pro603Arg)	rs63750876	0.00009
NM_000249.4(MLH1):c.649C>T (p.Arg217Cys)	rs4986984	0.00007
NM_000249.4(MLH1):c.2174G>A (p.Arg725His)	rs566928243	0.00006
NM_000249.4(MLH1):c.1128T>C (p.Asp376=)	rs267607824	0.00005
NM_000249.4(MLH1):c.303T>G (p.Gly101=)	rs4647220	0.00002
NM_000249.4(MLH1):c.1990-6G>A	rs117221851	0.00001
NM_000249.4(MLH1):c.2070C>T (p.Tyr690=)	rs550890395	0.00001
NM_000249.4(MLH1):c.24T>A (p.Ile8=)	rs748406142	0.00001
NM_000249.4(MLH1):c.*32CTT[1]	rs193922366
NM_000249.4(MLH1):c.1852_1853delinsGC (p.Lys618Ala)	rs35502531
NM_000249.4(MLH1):c.1853A>C (p.Lys618Thr)	rs63750449
NM_000249.4(MLH1):c.927C>T (p.Pro309=)	rs63749896

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