Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16260
CDH1
0.716 0.440 16 68737131 upstream gene variant C/A snv 0.24 18
rs9929218
CDH1
0.732 0.160 16 68787043 intron variant G/A snv 0.28 8
rs35187787
CDH1
0.827 0.120 16 68822063 missense variant G/A;T snv 3.3E-03; 2.4E-05 5
rs13689
CDH1
0.851 0.120 16 68834619 3 prime UTR variant T/A;C;G snv 4
rs746481984
CDH1
0.851 0.120 16 68819393 missense variant C/G;T snv 4.0E-06 4
rs7198799
CDH1
0.882 0.120 16 68784487 intron variant C/T snv 0.27 3
rs17715799
CDH1
0.882 0.120 16 68796608 intron variant A/G;T snv 3
rs12185157
CDH1
0.882 0.120 16 68750684 intron variant G/A;C;T snv 3
rs587780784
CDH1
1.000 0.080 16 68811854 stop gained C/G;T snv 1.6E-05; 8.0E-06 3
rs121964877
CDH1
0.851 0.160 16 68822081 stop gained C/G;T snv 3
rs5030625
CDH1
0.882 0.160 16 68736944 upstream gene variant A/- del 0.80 3
rs587782359
CDH1
1.000 0.080 16 68812244 missense variant C/G;T snv 2.8E-05 3
rs10431924
CDH1
0.882 0.120 16 68805399 intron variant T/C snv 0.45 3
rs876658146
CDH1
0.882 0.200 16 68815743 missense variant A/G snv 3
rs757422353
CDH1
0.882 0.200 16 68823432 missense variant C/G snv 4.0E-06 3
rs7200690
CDH1
0.925 0.080 16 68744554 intron variant C/T snv 0.23 2
rs786202482
CDH1
0.925 0.080 16 68815678 missense variant T/C snv 2.1E-05 2
rs1801026
CDH1
1.000 0.120 16 68833553 3 prime UTR variant C/A;G;T snv 2
rs587780537
CDH1
0.925 0.080 16 68810224 missense variant G/A snv 2
rs1060501248
CDH1
1.000 0.080 16 68829679 frameshift variant G/- delins 2
rs587781351
CDH1
1.000 0.040 16 68828263 missense variant G/A;C snv 4.0E-06; 4.0E-06 2
rs10431923
CDH1
0.925 0.120 16 68805360 intron variant G/T snv 0.44 2
rs4783689
CDH1
0.925 0.080 16 68819768 intron variant C/T snv 0.30 2
rs17690554
CDH1
0.925 0.080 16 68835607 downstream gene variant C/G;T snv 2
rs9939049
CDH1
0.790 0.080 16 68778398 intron variant A/T snv 0.29 1