Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4646903
CYP1A1
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 11
rs13212041
LOC105377864 ; HTR1B
0.851 0.200 6 77461407 downstream gene variant C/T snv 0.70 6
rs684846 1.000 0.120 3 183173176 downstream gene variant C/T snv 0.85 1
rs7218361 1.000 0.120 17 39569151 downstream gene variant A/G snv 0.97 1
rs8006998 1.000 0.120 14 75234687 downstream gene variant C/A;T snv 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs17300539
ADIPOQ
0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs2060793
CYP2R1
0.776 0.240 11 14893764 upstream gene variant A/G snv 0.63 11
rs2119882
MTNR1A
0.807 0.320 4 186555751 upstream gene variant T/C snv 0.57 9
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 7
rs4786370
IL32
0.882 0.280 16 3063897 upstream gene variant T/C snv 0.42 3
rs7312770 0.925 0.120 12 56073803 upstream gene variant C/T snv 0.53 2
rs10739076 1.000 0.120 9 5440589 upstream gene variant A/C;T snv 1
rs1423560
FST
1.000 0.120 5 53479932 upstream gene variant G/A;T snv 1
rs2002555
AMHR2
1.000 0.120 12 53423453 upstream gene variant A/G snv 0.16 1
rs6022786 1.000 0.120 20 53830764 upstream gene variant A/G snv 0.55 1