List of variants reported as benign for Colorectal cancer, susceptibility to, 12 by Counsyl

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_006231.4(POLE):c.6657+16C>T	rs5745075	0.34836
NM_006231.4(POLE):c.2550C>T (p.Ile850=)	rs5744834	0.01438
NM_006231.4(POLE):c.5678+4C>T	rs5744973	0.01405
NM_006231.4(POLE):c.91G>T (p.Ala31Ser)	rs34047482	0.01320
NM_006231.4(POLE):c.5804G>A (p.Cys1935Tyr)	rs5744991	0.00898
NM_006231.4(POLE):c.1007A>G (p.Asn336Ser)	rs5744760	0.00805
NM_006231.4(POLE):c.1470C>T (p.Asp490=)	rs5744777	0.00679
NM_006231.4(POLE):c.1359+9G>A	rs75135381	0.00498
NM_006231.4(POLE):c.6817A>T (p.Thr2273Ser)	rs73481453	0.00444
NM_006231.4(POLE):c.3275+16A>G	rs5744858	0.00004
NM_006231.4(POLE):c.2083T>A (p.Phe695Ile)	rs5744799
NM_006231.4(POLE):c.2865-5_2865-4del	rs369732588

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