Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799768
SERPINE1
0.807 0.360 7 101126425 upstream gene variant -/A;C ins 6
rs139876191
HMGA1
1.000 0.120 6 34242693 intron variant -/C delins 7.7E-02; 5.8E-06 5.2E-02 1
rs3134069
COLEC10 ; TNFRSF11B
0.776 0.320 8 118952749 upstream gene variant A/C snv 9.6E-02 11
rs1372503923
ITGA2
0.925 0.160 5 53048731 missense variant A/C snv 3
rs9896052 0.882 0.160 17 75422781 intergenic variant A/C snv 0.50 3
rs13163610
LOC105379087 ; KIAA0825
1.000 0.120 5 94213172 intron variant A/C snv 0.11 1
rs14259
PSMD9
0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
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
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs4636297
EGFL7 ; MIR126
0.724 0.360 9 136670698 intron variant A/G snv 0.67 0.65 14
rs6218
LINC02456 ; HELLPAR ; IGF1
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
rs5742612
LOC105369944 ; IGF1
0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02 11