Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1050106163
APOE
1.000 0.040 19 44908618 missense variant C/T snv 7.0E-06 1
rs1081105
APOE
1.000 0.080 19 44909698 non coding transcript exon variant A/C snv 3.0E-02 1
rs115299243
APOE
19 44907291 non coding transcript exon variant A/G snv 7.1E-03 1
rs11542029
APOE
1.000 0.080 19 44907864 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 1.2E-05 1
rs11542035
APOE
19 44908706 missense variant G/A snv 1.9E-05 2.8E-05 1
rs11542037
APOE
1.000 0.080 19 44908657 missense variant C/A;T snv 5.2E-06 1
rs11542041
APOE
0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs1167428194
APOE
1.000 0.080 19 44908634 missense variant A/C snv 1
rs121918392
APOE
0.925 0.040 19 44907777 missense variant G/A snv 3.6E-05 7.0E-06 2
rs121918393
APOE
0.851 0.120 19 44908756 missense variant C/A;T snv 1.3E-05; 9.0E-05 6
rs121918394
APOE
0.882 0.080 19 44908786 missense variant A/C;G snv 6.5E-06 5
rs121918395
APOE
19 44909032 missense variant C/A;T snv 6.9E-06; 4.2E-05 1
rs121918396
APOE
1.000 0.080 19 44908979 stop gained G/A snv 1.6E-05 3.5E-05 1
rs121918397
APOE
0.882 0.200 19 44908784 missense variant G/A;C snv 6.5E-06 3
rs121918398
APOE
19 44909171 missense variant G/A snv 4.5E-06 1
rs121918399
APOE
0.925 0.120 19 44907843 missense variant C/T snv 8.0E-06 2
rs1233347077
APOE
0.851 0.160 19 44905894 missense variant G/C snv 7.0E-06 4
rs1270059098
APOE
1.000 0.080 19 44906634 synonymous variant C/T snv 4.0E-06 1
rs1275147925
APOE
1.000 0.080 19 44906613 missense variant A/G snv 7.0E-06 1
rs1335550286
APOE
1.000 0.040 19 44909005 missense variant G/A snv 7.0E-06 2
rs140808909
APOE
0.851 0.120 19 44909080 missense variant G/A snv 2.0E-04 5.6E-05 5
rs1424027593
APOE
1.000 0.080 19 44908639 missense variant C/A snv 1
rs142480126
APOE
19 44907825 missense variant G/A snv 8.0E-06 1
rs1438607869
APOE
1.000 0.080 19 44908741 missense variant G/A snv 1
rs1440976751
APOE
1.000 0.080 19 44907789 missense variant G/A snv 1