Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 13
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 10
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 10
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 8
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 7
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 7
rs2927438 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 6
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 6
rs11755527
BACH2
0.851 0.360 6 90248512 intron variant C/G snv 0.36 5
rs12722495
IL2RA
0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 5
rs1701704
LOC105369781 ; IKZF4
0.851 0.200 12 56018703 intron variant T/G snv 0.25 5
rs3788013
UBASH3A
0.851 0.240 21 42421219 intron variant C/A snv 0.44 5