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

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_014239.4(EIF2B2):c.*180G>C	rs4556	0.45760
NM_001040108.2(MLH3):c.*3148A>G	rs108621	0.42508
NM_016467.5(ORMDL1):c.-118+190C>A	rs5742926	0.11427
NM_000179.2(MSH6):c.-159C>T	rs41540312	0.07535
NM_001040108.2(MLH3):c.*2965C>T	rs10134636	0.03135
NM_014239.4(EIF2B2):c.*3G>C	rs112087431	0.01958
NM_014239.4(EIF2B2):c.*56C>T	rs116393177	0.01153
NM_000249.4(MLH1):c.588+11G>C	rs4647258	0.00993
NM_001040108.2(MLH3):c.*3140C>T	rs77514025	0.00950
NM_000179.3(MSH6):c.4068_4071dup (p.Lys1358delinsAspTer)	rs55740729
NM_000249.4(MLH1):c.*158GATT[1]	rs796807655
NM_000249.4(MLH1):c.*32CTT[1]	rs193922366
NM_000535.6(PMS2):c.-93G>T	rs6976537
NM_001040108.2(MLH3):c.*1341del	rs5809689

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