Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs551238
EPO
0.925 0.160 7 100723905 downstream gene variant G/T snv 0.62 5
rs13064954 1.000 0.120 3 157136953 downstream gene variant G/A snv 7.9E-02 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
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
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
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs1617640
EPO
0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 15
rs1927914
TLR4
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52 14
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs3134069
COLEC10 ; TNFRSF11B
0.776 0.320 8 118952749 upstream gene variant A/C snv 9.6E-02 11
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs2514259
AIP
0.807 0.280 11 67479201 upstream gene variant C/G;T snv 8
rs1799768
SERPINE1
0.807 0.360 7 101126425 upstream gene variant -/A;C ins 6
rs13207351
VEGFA
0.851 0.280 6 43770057 upstream gene variant A/G;T snv 4
rs2808629 0.925 0.160 1 159707006 upstream gene variant G/A snv 0.31 3
rs3759890
SORD
0.925 0.160 15 45022396 upstream gene variant C/G snv 0.19 2
rs1145612 1.000 0.120 5 158271107 upstream gene variant C/A snv 0.49 1
rs12150053
SERPINF1
1.000 0.120 17 1761175 upstream gene variant T/A;C snv 1
rs12948385
SERPINF1
1.000 0.120 17 1761607 upstream gene variant G/A snv 0.26 1