List of variants reported as likely benign for Breast carcinoma

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.965G>A (p.Gly322Asp)	rs4987188	0.01714
NM_198253.3(TERT):c.3184G>A (p.Ala1062Thr)	rs35719940	0.01370
NM_000179.3(MSH6):c.3160A>T (p.Ile1054Phe)	rs267608075	0.00016
NM_000251.3(MSH2):c.1386+23T>G	rs747646424	0.00010
NM_000059.4(BRCA2):c.5455C>T (p.Pro1819Ser)	rs80358768	0.00009
NM_000249.4(MLH1):c.1039-8_1039-7insTA	rs535965616
NM_000251.3(MSH2):c.942+22_942+29del	rs11309117
NM_000264.5(PTCH1):c.110G>C (p.Gly37Ala)	rs748780206
NM_015450.3(POT1):c.702+8_702+9delinsTG	rs36069303

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