Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1794275 1.000 0.120 6 32703471 downstream gene variant G/A snv 0.21 2
rs2856717 1.000 0.120 6 32702531 downstream gene variant A/G snv 0.64 2
rs2738048 1.000 0.120 8 6965263 downstream gene variant A/G snv 0.28 1
rs2738081 1.000 0.120 8 6957996 downstream gene variant G/T snv 0.15 1
rs3129269 1.000 0.120 6 33129837 downstream gene variant C/A;T snv 1
rs4288398 1.000 0.120 8 7024116 downstream gene variant A/G snv 0.70 1
rs6984215 1.000 0.120 8 7027356 downstream gene variant T/C snv 0.30 1
rs7763262 1.000 0.120 6 32457105 downstream gene variant T/C snv 0.70 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1800875
CMA1
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41 12
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 8
rs9275596 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 7
rs11264799
FCRL3
0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28 6
rs10086568 1.000 0.120 8 7042814 upstream gene variant G/A snv 0.34 2
rs2523946
HCG9 ; HLA-A
0.925 0.200 6 29974166 upstream gene variant C/A;G;T snv 2
rs2738058 0.925 0.160 8 6964095 upstream gene variant T/C snv 0.57 2
rs12716641 1.000 0.120 8 7041476 upstream gene variant T/A;C snv 1
rs2615787 1.000 0.120 8 6953627 upstream gene variant T/G snv 0.41 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs140433921
SLC3A1
1.000 0.120 2 44286102 start lost T/C snv 2.0E-05 5.6E-05 1
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 5
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38