Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs11568818
MMP7
0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 15
rs11200638
LOC105378525 ; HTRA1
0.724 0.280 10 122461028 non coding transcript exon variant G/A snv 0.23 14
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs2146323
VEGFA
0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 9
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54 9
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs57137919
ABCG1 ; LOC105372814
0.776 0.160 21 42218908 intron variant G/A snv 0.14 9
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 7
rs10922109
CFH
0.827 0.080 1 196735502 intron variant C/A snv 0.46 6
rs1142
SRPK2
0.851 0.040 7 105115879 intron variant C/T snv 0.31 6
rs570618
CFH
0.827 0.040 1 196687934 intron variant T/G snv 0.69 6
rs79037040
TNFRSF10A ; LOC389641
0.807 0.160 8 23225458 non coding transcript exon variant G/A;C;T snv 6
rs943080
LOC107986598
0.807 0.040 6 43858890 TF binding site variant C/T snv 0.61 6
rs11080055
TMEM97
0.851 0.040 17 28322698 intron variant A/C snv 0.54 5
rs114254831
PBX2
0.827 0.040 6 32187804 intron variant A/G snv 5
rs116503776
CYP21A2 ; SKIV2L
0.827 0.040 6 31962685 intron variant G/A snv 5
rs13095226
COL8A1
0.851 0.040 3 99677428 intron variant T/C snv 9.5E-02 5