Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1417938
CRP
0.776 0.320 1 159714396 intron variant T/A;C snv 0.28 10
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 10
rs2479409
PCSK9
1.000 0.040 1 55038977 upstream gene variant G/A snv 0.66 4
rs12133641
IL6R
0.925 0.040 1 154455807 intron variant A/G snv 0.44 3
rs4916251
DNM3 ; PIGC
0.882 0.040 1 172377256 intron variant T/A snv 0.70 3
rs1795061 1.000 0.040 1 214235937 intergenic variant T/C;G snv 1
rs6674171
TDRD10
1.000 0.040 1 154519207 intron variant A/G;T snv 0.19 1
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs12692386
ADAM17
0.827 0.160 2 9555777 5 prime UTR variant A/G snv 0.72 5
rs1524668
ADAM17
0.851 0.160 2 9557243 upstream gene variant A/C snv 0.64 4
rs919433
ANKRD44 ; ANKRD44-IT1
0.882 0.080 2 197301841 intron variant G/A snv 0.38 3
rs1057518075
MIR3606 ; COL3A1
1.000 0.040 2 188995061 stop gained C/T snv 1
rs13382862
LDAH
1.000 0.040 2 20682689 upstream gene variant A/G;T snv 0.59 1
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38