Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1060501214
CDH1
1.000 0.080 16 68810201 frameshift variant TC/- delins 1
rs1060501215
CDH1
1.000 0.080 16 68801878 frameshift variant C/- delins 1
rs1060501224
CDH1
1.000 0.080 16 68822180 frameshift variant AC/- delins 1
rs1060501226
CDH1
1.000 0.080 16 68738295 splice acceptor variant A/G snv 1
rs1060501237
CDH1
1.000 0.080 16 68811861 splice donor variant T/C snv 1
rs1060501248
CDH1
1.000 0.080 16 68829679 frameshift variant G/- delins 1
rs1064794231
CDH1
1.000 0.080 16 68810240 missense variant A/G snv 7.0E-06 1
rs1064795267
CDH1
1.000 0.080 16 68815760 splice donor variant G/- del 1
rs1064795703
CDH1
1.000 0.080 16 68801820 frameshift variant C/- delins 1
rs121964874
CDH1
1.000 0.080 16 68823557 stop gained C/A;G;T snv 4.0E-06 1
rs121964875
CDH1
1.000 0.080 16 68738307 stop gained G/A snv 1
rs121964876
CDH1
1.000 0.080 16 68738318 stop gained G/T snv 1
rs121964878
CDH1
1.000 0.080 16 68822190 missense variant C/T snv 1
rs1375617541
CDH1
1.000 0.080 16 68829739 frameshift variant -/C delins 4.0E-06 1
rs1440280370
CDH1
1.000 0.080 16 68737464 splice donor variant G/A;T snv 1
rs149127230
CDH1
1.000 0.080 16 68823566 stop gained G/A;C;T snv 1.7E-04; 4.0E-06 1
rs1555509622
CDH1
1.000 0.080 16 68737416 start lost A/G snv 1
rs1555509636
CDH1
1.000 0.080 16 68737427 stop gained G/A snv 1
rs1555514406
CDH1
1.000 0.080 16 68801709 frameshift variant -/T delins 1
rs1555514429
CDH1
1.000 0.080 16 68801766 frameshift variant G/- delins 1
rs1555515215
CDH1
1.000 0.080 16 68808503 stop gained G/A snv 1
rs1555515284
CDH1
1.000 0.080 16 68808816 frameshift variant C/- delins 1
rs1555515297
CDH1
1.000 0.080 16 68808850 splice donor variant T/C snv 1
rs1555515596
CDH1
1.000 0.080 16 68811682 splice acceptor variant A/G snv 1
rs1555515726
CDH1
1.000 0.080 16 68812177 stop gained C/T snv 1