List of variants reported as likely benign for Lynch syndrome 2 by Illumina Laboratory Services, Illumina

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Total variants: 12

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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.474C>T (p.Asn158=)	rs4647256	0.01161
NM_000249.4(MLH1):c.637G>A (p.Val213Met)	rs2308317	0.00818
NM_000249.4(MLH1):c.589-15C>T	rs55658850	0.00582
NM_000249.4(MLH1):c.1852A>G (p.Lys618Glu)	rs35001569	0.00399
NM_000249.4(MLH1):c.1963A>G (p.Ile655Val)	rs55907433	0.00297
NM_000249.4(MLH1):c.1151T>A (p.Val384Asp)	rs63750447	0.00077
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.2066A>G (p.Gln689Arg)	rs63750702	0.00022
NM_000249.4(MLH1):c.303T>G (p.Gly101=)	rs4647220	0.00002
NM_000249.4(MLH1):c.*32C>T	rs200903126

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