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
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 8
rs6024836
FAM210B ; AURKA
0.851 0.160 20 56369012 downstream gene variant G/A snv 0.42 7
rs2069852 0.925 0.080 7 22732641 downstream gene variant G/A;C snv 4
rs1469557
LOC101929248
0.925 0.120 8 10849291 downstream gene variant C/T snv 0.18 2
rs3094137 0.925 0.120 6 30233096 downstream gene variant A/G;T snv 2
rs4309483 0.925 0.120 18 58418685 downstream gene variant A/C snv 0.70 2
rs4985790 0.925 0.120 17 21420842 downstream gene variant G/A snv 2
rs12309362 1.000 0.080 12 132466447 downstream gene variant G/A;T snv 1
rs2064836 1.000 0.080 X 92628018 downstream gene variant A/G;T snv 1
rs7821974 1.000 0.080 8 37592483 downstream gene variant T/C snv 0.22 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
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs3834129
CASP8
0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs2853669
TERT
0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33