Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs4796793
STAT3
0.716 0.320 17 42390192 upstream gene variant G/C snv 0.67 16
rs4646437
CYP3A4
0.827 0.200 7 99767460 intron variant G/A snv 0.30 8
rs9582036
FLT1
0.776 0.280 13 28311271 intron variant C/A snv 0.59 8
rs34231037
KDR
0.882 0.160 4 55106779 missense variant A/G snv 2.3E-02 2.3E-02 7
rs9554320
FLT1
0.882 0.160 13 28312790 intron variant A/C;G snv 3