Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs1950902
MTHFD1
0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11
rs2149954
LINC02227
0.882 0.080 5 158393594 intron variant C/T snv 0.37 5
rs3212335
GABRB3 ; LOC112268151
1.000 0.080 15 26766994 intron variant C/T snv 0.32 4
rs6489785 1.000 0.040 12 120925921 TF binding site variant T/C snv 0.68 3
rs739401
CARS1
11 3015094 intron variant C/T snv 0.45 2
rs1262476
LOC105377992
6 126665850 intron variant A/G;T snv 2
rs2516739
NTHL1 ; TSC2
16 2047157 non coding transcript exon variant G/A snv 0.30 2
rs2758603
PMF1-BGLAP ; PMF1
1 156229203 intron variant T/C snv 0.37 2
rs10934524 3 96431316 intergenic variant C/G;T snv 1
rs12143832 1 21378943 regulatory region variant T/C snv 0.44 1
rs138762279 5 174283195 intergenic variant T/- del 0.34 1
rs1416280 6 102438768 intergenic variant C/G snv 0.35 1
rs1425609 3 162964207 intergenic variant G/A snv 0.37 1
rs145672791 21 13377702 intergenic variant G/A snv 8.1E-03 1
rs1487614 4 42267463 non coding transcript exon variant T/C snv 0.65 1
rs2031577 10 4007811 intergenic variant A/G snv 0.53 1
rs2882281 13 89970201 intergenic variant C/A;G;T snv 1
rs3106598 13 61104778 intron variant G/A snv 0.43 1
rs6813479 4 136739228 intergenic variant T/A;C snv 1
rs6915183 6 166292681 intergenic variant A/G;T snv 1