Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 10
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 7
rs4240807 0.851 0.160 16 85951755 downstream gene variant A/C snv 0.76 4
rs12630450 1.000 0.160 3 169762416 downstream gene variant A/G snv 0.33 2
rs12864436
LOC105370120
0.925 0.200 13 25103371 downstream gene variant A/G snv 0.40 2
rs1555902 1.000 0.160 13 108204435 downstream gene variant C/A snv 0.10 1
rs7634985 1.000 0.160 3 41978073 downstream gene variant C/T snv 0.72 1
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs733618
CTLA4
0.763 0.440 2 203866221 upstream gene variant T/C snv 0.10 12
rs13069553 0.851 0.200 3 169790484 upstream gene variant A/G snv 0.21 4
rs1672753
CRBN
0.882 0.240 3 3179746 upstream gene variant C/T snv 0.71 4
rs2107356
IL4R
0.851 0.240 16 27312083 upstream gene variant C/T snv 0.35 4
rs10936602
LRRIQ4
0.882 0.240 3 169818849 upstream gene variant T/C snv 0.26 3
rs12584389 0.925 0.200 13 79801869 upstream gene variant T/C snv 4.4E-02 2
rs3821383
MYNN
1.000 0.160 3 169772158 upstream gene variant A/C;G;T snv 2
rs6768972
CRBN
1.000 0.160 3 3180101 upstream gene variant A/C;G snv 2
rs7633750 1.000 0.160 3 169791456 upstream gene variant G/A snv 0.38 2
rs9856633 1.000 0.160 3 41972358 upstream gene variant A/G snv 0.68 2
rs10510732 1.000 0.160 3 41965847 upstream gene variant G/A snv 0.12 1
rs113144620 1.000 0.160 3 41966820 upstream gene variant A/G snv 0.13 1
rs113379006 1.000 0.160 3 41966694 upstream gene variant C/T snv 0.13 1
rs12158877
CBX7
1.000 0.160 22 39153421 upstream gene variant T/G snv 0.45 1
rs12492599
ULK4
1.000 0.160 3 41964242 upstream gene variant C/A snv 0.67 1
rs3130454
PSORS1C2
1.000 0.160 6 31140708 upstream gene variant G/A snv 0.71 1