Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs689466
PACERR ; PTGS2
0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs57095329
MIR3142HG
0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs11134527
MIR218-2 ; SLIT3
0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs1412125
HMGB1
0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs12041331
PEAR1
0.776 0.200 1 156899922 intron variant G/A snv 0.19 11
rs3118470
IL2RA
0.752 0.360 10 6059750 intron variant T/A;C snv 10
rs2287886
CD209
0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs2516400 0.827 0.320 6 31513328 upstream gene variant G/A snv 0.32 8
rs3755724
TIMP4 ; SYN2
0.790 0.360 3 12159406 intron variant C/T snv 0.31 8
rs5050
AGT
0.827 0.200 1 230714140 intron variant T/C;G snv 7
rs6906846
HLA-B ; USP8P1
0.851 0.280 6 31277959 non coding transcript exon variant A/G snv 0.67 7
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 6
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 6
rs7812879 0.807 0.320 8 11482672 upstream gene variant T/A;C snv 6
rs1600249
BLK
0.827 0.280 8 11502129 intron variant G/T snv 0.23 5
rs2070676
CYP2E1
0.827 0.320 10 133537633 non coding transcript exon variant G/C snv 0.73 5