Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2249825
HMGB1
0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs1057518731
SMARCD2
0.807 0.280 17 63833908 splice donor variant C/T snv 7
rs1057518733
SMARCD2
0.807 0.280 17 63837439 splice donor variant A/G snv 7
rs879253740
NPC2 ; ISCA2
0.882 0.240 14 74493191 splice donor variant A/G snv 5
rs1045411
HMGB1
0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 18
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs796051877
GAA
0.807 0.320 17 80110055 splice region variant G/A snv 4.0E-06 11
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169