Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1008563 1.000 0.080 2 218162165 downstream gene variant G/A snv 0.43 1
rs10176176 1.000 0.080 2 85534925 upstream gene variant A/T snv 0.54 1
rs17708087 1.000 0.080 17 40514261 upstream gene variant A/G snv 0.15 1
rs2019090 1.000 0.080 11 103798234 intron variant A/C;G;T snv 1
rs2315065 1.000 0.080 6 160687112 intergenic variant C/A;T snv 1
rs490556 1.000 0.080 5 4022536 intergenic variant G/A snv 0.57 1
rs521660 1.000 0.080 5 4035819 intron variant T/C snv 0.61 1
rs6941513 1.000 0.080 6 163609768 intergenic variant A/G snv 0.45 1
rs7211079 1.000 0.080 17 80133738 downstream gene variant A/G snv 0.29 1
rs822387 1.000 0.080 3 186838248 upstream gene variant T/C snv 0.15 1
rs13301354
ABCA2 ; FUT7 ; C9orf139
1.000 0.080 9 137030185 3 prime UTR variant T/C snv 0.64 1
rs9635480
ABCC1
1.000 0.080 16 16000744 intron variant A/G snv 0.50 1
rs6138473
ACSS1
1.000 0.080 20 25031519 intron variant C/T snv 0.38 1
rs2275725
ADAM8
1.000 0.080 10 133275531 missense variant A/G snv 0.89 0.90 1
rs2995300
ADAM8
1.000 0.080 10 133263019 3 prime UTR variant C/A snv 0.87 0.83 1
rs72563731
ADIPOQ ; ADIPOQ-AS1
1.000 0.080 3 186854292 missense variant C/T snv 1.6E-05 2.3E-04 1
rs200741295
ADORA2B
1.000 0.080 17 15975230 missense variant A/G;T snv 1.3E-04; 4.0E-06 7.0E-06 1
rs761660984
AHSG
1.000 0.080 3 186620589 missense variant G/A;C;T snv 2.9E-05 1
rs3803915
AP3D1
1.000 0.080 19 2160530 intron variant C/A;T snv 1
rs369066087
APOA1-AS ; APOA1
1.000 0.080 11 116837117 synonymous variant G/A;C snv 2.0E-05 2.8E-05 1
rs1135402763
APOB
1.000 0.080 2 21032540 missense variant T/C;G snv 1
rs1275147925
APOE
1.000 0.080 19 44906613 missense variant A/G snv 7.0E-06 1
rs1458301734
APOE
1.000 0.080 19 44908687 missense variant G/A;T snv 5.9E-06 1
rs868094551
APOE
1.000 0.080 19 44908768 missense variant C/A;T snv 1
rs17599586
ARG1 ; MED23
1.000 0.080 6 131583579 intron variant C/T snv 0.11 1