List of variants studied for hereditary gastric cancer by OMIM

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Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_004360.5(CDH1):c.1849G>A (p.Ala617Thr)	rs33935154	0.01412
NM_004360.5(CDH1):c.1018A>G (p.Thr340Ala)	rs116093741	0.00022
NM_004360.5(CDH1):c.2494G>A (p.Val832Met)	rs35572355	0.00004
NM_001127511.3(APC):c.-192A>G	rs879253784	0.00001
NC_000016.10:g.68602418_68796011del
NM_001127511.2(APC):c.[-125delA;-195A>C]
NM_001127511.3(APC):c.-191T>C	rs879253783
NM_004360.5(CDH1):c.1008G>T (p.Glu336Asp)	rs267606712
NM_004360.5(CDH1):c.1590dup (p.Asn531fs)	rs1555516535
NM_004360.5(CDH1):c.1711+1dup	rs2152137028
NM_004360.5(CDH1):c.1792C>T (p.Arg598Ter)	rs121964877
NM_004360.5(CDH1):c.1901C>T (p.Ala634Val)	rs121964878
NM_004360.5(CDH1):c.2095C>T (p.Gln699Ter)	rs121964874
NM_004360.5(CDH1):c.2386dup (p.Arg796fs)	rs1375617541
NM_004360.5(CDH1):c.2440-396_*224delinsGGA	rs2152143625
NM_004360.5(CDH1):c.49-2A>G	rs1060501226
NM_004360.5(CDH1):c.521dup (p.Asn174fs)	rs587781290
NM_004360.5(CDH1):c.59G>A (p.Trp20Ter)	rs121964875
NM_004360.5(CDH1):c.70G>T (p.Glu24Ter)	rs121964876

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