Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 8
rs2737190 0.827 0.120 9 117701903 upstream gene variant G/A snv 0.52 6
rs7194886 0.851 0.080 16 50691282 upstream gene variant C/T snv 0.38 4
rs4331426 0.925 0.080 18 22610832 intergenic variant G/A snv 0.86 2
rs4788172 0.925 0.120 16 29656932 regulatory region variant G/A snv 0.12 2
rs1568952 1.000 0.080 8 58799804 intergenic variant T/C snv 0.75 1
rs6507226 1.000 0.080 18 22611328 intergenic variant A/G snv 0.45 1
rs9271300 1.000 0.080 6 32613805 intergenic variant C/G snv 0.54 1
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1800870
ALDH3A2
0.851 0.200 17 19649164 intron variant C/T snv 5
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2072069
CCL13
0.925 0.120 17 34357972 intron variant G/A snv 0.47 2
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs4804803
CD209
0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs373950030
CD209
0.882 0.080 19 7744967 missense variant C/T snv 2.0E-05 2.1E-05 3
rs3211956
CD36
0.925 0.160 7 80674446 intron variant T/G snv 6.7E-02 3
rs10499859
CD36
0.925 0.120 7 80629494 intron variant A/G snv 0.46 2
rs1194182
CD36
1.000 0.080 7 80602188 5 prime UTR variant G/C snv 0.53 2
rs3092923
CD40LG
1.000 0.080 X 136659026 intron variant T/C snv 0.17 0.28 1
rs6768300
CISH ; MAPKAPK3
0.925 0.120 3 50611939 5 prime UTR variant C/G snv 0.85 2
rs10841845
CLEC4E
0.925 0.200 12 8533837 3 prime UTR variant A/G snv 0.28 2
rs10841847
CLEC4E
1.000 0.080 12 8535216 intron variant A/G snv 0.58 1
rs34069356
CTSZ
0.925 0.080 20 58995705 missense variant C/T snv 1.1E-03 4.3E-03 2