Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3785859
BCAS3
1.000 0.040 17 61302377 intron variant A/C snv 0.46 1
rs56184183
MMP12
1.000 0.040 11 102863081 3 prime UTR variant A/C snv 1.1E-03 1.0E-03 1
rs6481619
SVIL
1.000 0.040 10 29694025 intron variant A/C snv 0.25 1
rs76351433
LINC01118
1.000 0.040 2 46795404 intron variant A/C snv 6.8E-02 1
rs76677753 1.000 0.040 15 34605865 intergenic variant A/C snv 7.0E-03 1
rs2089162
IREB2
1.000 0.040 15 78447421 intron variant A/C;G snv 3
rs10922104
CFH
1.000 0.040 1 196718600 intron variant A/C;G snv 2
rs11174267
TAFA2
1.000 0.040 12 61992819 intron variant A/C;G snv 0.29 2
rs11640875
MIR8058 ; CDH13
1.000 0.040 16 82687819 intron variant A/C;G snv 1
rs117261012
ME3-DT
1.000 0.040 11 86733719 intron variant A/C;G snv 0.11 1
rs145442019
HSBP1
1.000 0.040 16 83811073 intron variant A/C;G snv 1
rs56036015
TNF
1.000 0.040 6 31575287 upstream gene variant A/C;G snv 7.0E-06; 1.4E-05 1
rs4713916
FKBP5
0.790 0.160 6 35702206 intron variant A/C;G;T snv 11
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1008438
HSPA1L ; HSPA1A
0.807 0.120 6 31815431 upstream gene variant A/C;T snv 6
rs10922105
CFH
1.000 0.040 1 196721120 intron variant A/C;T snv 2
rs475937
WTAPP1
1.000 0.040 11 102816969 intron variant A/C;T snv 2
rs688258
WTAPP1
1.000 0.040 11 102821364 intron variant A/C;T snv 2
rs2096468 1.000 0.040 21 34289445 intron variant A/C;T snv 1
rs68120025 1.000 0.040 17 71077504 intergenic variant A/C;T snv 1
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92