List of variants reported as uncertain significance for Colorectal cancer, susceptibility to, 10 by Mendelics

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_002691.4(POLD1):c.1795G>A (p.Ala599Thr)	rs149569984	0.00026
NM_002691.4(POLD1):c.2388+5G>A	rs750085275	0.00009
NM_002691.4(POLD1):c.3016G>A (p.Ala1006Thr)	rs376197467	0.00003
NM_002691.4(POLD1):c.132G>A (p.Met44Ile)	rs757575448	0.00002
NM_002691.4(POLD1):c.1289A>G (p.Asn430Ser)	rs546554950	0.00001
NM_002691.4(POLD1):c.327G>C (p.Gln109His)	rs750260438	0.00001
NM_002691.4(POLD1):c.189G>T (p.Glu63Asp)	rs776773005
NM_002691.4(POLD1):c.208G>T (p.Val70Phe)	rs147911699
NM_002691.4(POLD1):c.2449C>G (p.Arg817Gly)	rs148176230
NM_002691.4(POLD1):c.3073G>A (p.Val1025Met)	rs1060501858

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