List of variants reported as benign for hereditary gastric cancer by KCCC/NGS Laboratory, Kuwait Cancer Control Center

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Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_004360.5(CDH1):c.48+6C>T	rs3743674	0.80384
NM_004360.5(CDH1):c.2076T>C (p.Ala692=)	rs1801552	0.70379
NM_004360.5(CDH1):c.1937-13T>C	rs2276330	0.09635
NM_004360.5(CDH1):c.531+10G>C	rs33963999	0.03907
NM_004360.5(CDH1):c.2253C>T (p.Asn751=)	rs33964119	0.03869
NM_004360.5(CDH1):c.48+5C>G	rs77312180	0.03370
NM_004360.5(CDH1):c.1896C>T (p.His632=)	rs33969373	0.02054
NM_004360.5(CDH1):c.2634C>T (p.Gly878=)	rs2229044	0.01638
NM_004360.5(CDH1):c.933C>G (p.Leu311=)	rs35539711	0.00974
NM_004360.5(CDH1):c.-71C>G	rs34033771	0.00927
NM_004360.5(CDH1):c.2439+22C>T	rs34751606	0.00346
NM_004360.5(CDH1):c.1680G>C (p.Thr560=)	rs35741240	0.00261
NM_004360.5(CDH1):c.324A>G (p.Arg108=)	rs116542018	0.00255
NM_004360.5(CDH1):c.345G>A (p.Thr115=)	rs1801023	0.00236
NM_004360.5(CDH1):c.-54G>C	rs5030874	0.00208
NM_004360.5(CDH1):c.2292C>T (p.Asp764=)	rs61747636	0.00159
NM_004360.5(CDH1):c.2440-6C>G	rs139757930	0.00145
NM_004360.5(CDH1):c.2520C>T (p.Ser840=)	rs140328601	0.00064
NM_004360.5(CDH1):c.1138-3C>T	rs36103202	0.00042
NM_004360.5(CDH1):c.1239C>T (p.Tyr413=)	rs36074916	0.00041
NM_004360.5(CDH1):c.670C>T (p.Arg224Cys)	rs200310662	0.00021
NM_004360.5(CDH1):c.1371G>A (p.Thr457=)	rs370368644	0.00003
NM_004360.5(CDH1):c.759C>T (p.Thr253=)	rs372934565	0.00003
NM_004360.5(CDH1):c.1773C>T (p.Asn591=)	rs373719554	0.00001
NM_004360.5(CDH1):c.604G>A (p.Val202Ile)	rs546716073	0.00001
NM_004360.5(CDH1):c.832+9A>T	rs1057521268	0.00001
NM_004360.5(CDH1):c.1308G>A (p.Leu436=)	rs557551011
NM_004360.5(CDH1):c.1680G>A (p.Thr560=)	rs35741240

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