Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6024836
FAM210B ; AURKA
0.851 0.160 20 56369012 downstream gene variant G/A snv 0.42 7
rs12881063
LOC107984671 ; LOC105370397
1.000 0.080 14 20788017 downstream gene variant G/C snv 7.4E-02 3
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
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
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs2295080
MTOR
0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 16
rs1800544
ADRA2A
0.790 0.160 10 111076745 upstream gene variant G/C snv 0.59 12
rs931127
SIPA1 ; PCNX3
0.790 0.160 11 65637829 upstream gene variant G/A snv 0.49 12
rs2494752
AKT1
0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs3219175
RETN
0.807 0.240 19 7668969 upstream gene variant G/A snv 5.0E-02 10
rs653765
ADAM10
0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45 10
rs2119882
MTNR1A
0.807 0.320 4 186555751 upstream gene variant T/C snv 0.57 9
rs10814325
RECK
0.827 0.200 9 36036597 upstream gene variant T/A;C;G snv 7
rs1536309
MIR146B
0.851 0.160 10 102435445 upstream gene variant A/G snv 0.32 7
rs6691378
CHI3L1
0.882 0.160 1 203187994 upstream gene variant G/A snv 0.19 6
rs10491121
LOC101927369 ; CCL4
0.882 0.120 17 36102943 upstream gene variant G/A snv 0.32 5
rs10420252
COX6B1
1.000 0.080 19 35648270 upstream gene variant G/A snv 9.7E-02 2
rs2118593
RYBP
1.000 0.080 3 72447740 upstream gene variant G/A;C;T snv 2
rs6475526 1.000 0.080 9 21242162 upstream gene variant C/T snv 0.33 2
rs6510502
COX6B1
1.000 0.080 19 35647577 upstream gene variant A/C;G snv 2