Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 16
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs17300539
ADIPOQ
0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs3134069
COLEC10 ; TNFRSF11B
0.776 0.320 8 118952749 upstream gene variant A/C snv 9.6E-02 11
rs11771443
NOS3
0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 8
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs5082
APOA2
0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 8
rs17111503
PCSK9
0.925 0.160 1 55037775 upstream gene variant A/G snv 0.22 7
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 7
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 7
rs2236418
GAD2
0.882 0.120 10 26216567 upstream gene variant A/G snv 0.36 6
rs2854117
APOC3
0.851 0.200 11 116829426 upstream gene variant T/A;C snv 6
rs12922822
UMOD
1.000 0.040 16 20356323 upstream gene variant C/A;T snv 5
rs1967017 0.882 0.160 1 145711421 upstream gene variant A/G snv 0.43 5
rs6499863 0.925 0.080 16 56958105 upstream gene variant G/A snv 0.19 5
rs1264347
LINC00243
1.000 0.040 6 30830920 upstream gene variant C/T snv 7.9E-02 4
rs13191445 0.925 0.120 6 26015261 upstream gene variant G/A snv 5.6E-02 4