List of variants reported as likely benign for carcinoma of esophagus

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_016373.4(WWOX):c.517-108230A>G	rs77067228	0.05744
NM_016373.4(WWOX):c.107+252C>T	rs58108921	0.00633
NM_005215.4(DCC):c.1062C>T (p.Val354=)	rs141716650	0.00555
NM_005215.4(DCC):c.2053+9T>C	rs186819956	0.00534
NM_016373.4(WWOX):c.1134C>T (p.Asn378=)	rs201088847	0.00274
NM_003242.6(TGFBR2):c.1119G>A (p.Met373Ile)	rs35719192	0.00130
NM_003242.6(TGFBR2):c.1458C>T (p.Ser486=)	rs139881155	0.00075
NM_003242.6(TGFBR2):c.571G>A (p.Val191Ile)	rs56105708	0.00039
NM_003242.6(TGFBR2):c.263+17A>C	rs34771516	0.00029
NM_000059.4(BRCA2):c.3445A>G (p.Met1149Val)	rs80358589	0.00013
NM_003242.6(TGFBR2):c.94+16238C>T	rs149757320	0.00013
NM_003242.6(TGFBR2):c.927G>A (p.Thr309=)	rs756625146	0.00002
NM_003242.6(TGFBR2):c.1208G>A (p.Arg403His)	rs143095746	0.00001
NM_000546.6(TP53):c.576G>C (p.Gln192His)	rs2073344721
NM_005215.4(DCC):c.2158C>T (p.Leu720=)	rs138143831

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