Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs115299243
APOE
19 44907291 non coding transcript exon variant A/G snv 7.1E-03 1
rs11542035
APOE
19 44908706 missense variant G/A snv 1.9E-05 2.8E-05 1
rs121918395
APOE
19 44909032 missense variant C/A;T snv 6.9E-06; 4.2E-05 1
rs121918398
APOE
19 44909171 missense variant G/A snv 4.5E-06 1
rs142480126
APOE
19 44907825 missense variant G/A snv 8.0E-06 1
rs200703101
APOE
19 44908757 missense variant G/C;T snv 1
rs28931576
APOE
19 44907894 missense variant A/G snv 1.2E-05 1.4E-05 1
rs28931578
APOE
19 44908751 missense variant G/A;C;T snv 3.2E-05 1
rs28931579
APOE
19 44909236 missense variant A/C snv 9.5E-05 6.3E-05 1
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs11542041
APOE
0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs267606661
APOE
0.763 0.120 19 44909101 missense variant C/G;T snv 3.9E-04; 1.0E-05 10
rs764929617
APOE
0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06 8
rs573658040
APOE
0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 9
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60 8
rs769455
APOE
0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03 8
rs121918393
APOE
0.851 0.120 19 44908756 missense variant C/A;T snv 1.3E-05; 9.0E-05 6
rs140808909
APOE
0.851 0.120 19 44909080 missense variant G/A snv 2.0E-04 5.6E-05 5
rs267606664
APOE
0.851 0.120 19 44908730 missense variant G/A;C snv 1.6E-04; 6.3E-06 5
rs1233347077
APOE
0.851 0.160 19 44905894 missense variant G/C snv 7.0E-06 4
rs752600356
APOE
0.851 0.280 19 44908681 missense variant G/A;C snv 2.3E-05 1.4E-05 4
rs769449
APOE
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 11
rs769446
APOE
0.882 0.120 19 44905371 upstream gene variant T/C snv 7.0E-02 6