Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs6465825 1.000 0.080 7 77787122 downstream gene variant T/C snv 0.41 4
rs10178409 1.000 0.080 2 73628380 downstream gene variant G/T snv 0.26 2
rs6587640
S100A10
1.000 0.080 1 151982754 downstream gene variant C/T snv 0.37 2
rs2880072 6 159404417 downstream gene variant G/A snv 0.49 1
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs2333227
MPO
0.752 0.320 17 58281401 upstream gene variant C/T snv 0.24 15
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs3134069
COLEC10 ; TNFRSF11B
0.776 0.320 8 118952749 upstream gene variant A/C snv 9.6E-02 11
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 7
rs12922822
UMOD
1.000 0.040 16 20356323 upstream gene variant C/A;T snv 5
rs12313273
ORAI1
0.882 0.160 12 121625105 upstream gene variant T/C snv 0.23 4
rs2575390
PRKCB
0.925 0.080 16 23835433 upstream gene variant G/A;C snv 3
rs3760106
PRKCB
0.925 0.080 16 23834475 upstream gene variant C/T snv 0.23 3
rs2393778 1.000 0.080 12 120702516 upstream gene variant G/C;T snv 2
rs3093058
CRP
1 159715525 upstream gene variant T/A;C;G snv 2
rs8101881 19 32873722 upstream gene variant C/T snv 0.54 2
rs270184 5 5124466 upstream gene variant C/A;T snv 1
rs78351985
C4orf54
4 99655532 upstream gene variant A/G snv 3.2E-04 1
rs754279998
MKS1
0.776 0.360 17 58208153 inframe deletion GAG/- delins 2.0E-05 1.4E-05 10
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs3752462
MYH9
0.827 0.160 22 36314138 splice region variant T/C snv 0.57 0.53 7