List of variants reported as benign for colorectal cancer by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_000535.7(PMS2):c.780C>G (p.Ser260=)	rs1805319	0.82058
NM_000251.3(MSH2):c.211+9C>G	rs2303426	0.55454
NM_000249.4(MLH1):c.1668-19A>G	rs9876116	0.41821
NM_000251.3(MSH2):c.1661+12G>A	rs3732183	0.40290
NM_000535.7(PMS2):c.705+17A>G	rs62456182	0.33782
NM_000179.3(MSH6):c.3438+14A>T	rs2020911	0.32279
NM_000179.3(MSH6):c.540T>C (p.Asp180=)	rs1800935	0.23857
NM_000249.4(MLH1):c.655A>G (p.Ile219Val)	rs1799977	0.23048
NM_000179.3(MSH6):c.116G>A (p.Gly39Glu)	rs1042821	0.18742
NM_000179.3(MSH6):c.276A>G (p.Pro92=)	rs1800932	0.14697
NM_000535.7(PMS2):c.2007-4G>A	rs1805326	0.12350
NM_000251.3(MSH2):c.1511-9A>T	rs12998837	0.09123
NM_000251.3(MSH2):c.2006-6T>C	rs2303428	0.08349
NM_000179.3(MSH6):c.642C>T (p.Tyr214=)	rs1800937	0.07457
NM_000535.7(PMS2):c.59G>A (p.Arg20Gln)	rs10254120	0.07445
NM_000249.4(MLH1):c.1558+14G>A	rs41562513	0.05554
NM_000535.7(PMS2):c.288C>T (p.Ala96=)	rs12532895	0.03944
NM_000535.7(PMS2):c.1866G>A (p.Met622Ile)	rs1805324	0.01651
NM_000251.3(MSH2):c.1077-10T>C	rs17224360	0.01428
NM_000249.4(MLH1):c.1039-8T>A	rs193922367	0.01153
NM_000535.7(PMS2):c.52A>G (p.Ile18Val)	rs63750123	0.00861
NM_000179.3(MSH6):c.2633T>C (p.Val878Ala)	rs2020912	0.00448
NM_000179.3(MSH6):c.3439-16C>T	rs192614006	0.00237
NM_000249.4(MLH1):c.790+10A>G	rs182733777	0.00188
NM_000535.7(PMS2):c.2324A>G (p.Asn775Ser)	rs17420802	0.00025
NM_000535.7(PMS2):c.*17G>C	rs556089649	0.00004
NM_000179.3(MSH6):c.3557-4dup	rs267608102
NM_000179.3(MSH6):c.4002-10del	rs59056100
NM_000535.7(PMS2):c.706-4del	rs60794673

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