Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs80356779
CPT1A
0.776 0.320 11 68780662 missense variant G/A snv 3.2E-05 5.6E-05 10
rs5030717
TLR4
0.807 0.240 9 117711556 intron variant A/G snv 0.13 9
rs1800028
FUT2 ; LOC105447645
0.925 0.040 19 48703560 stop gained C/G;T snv 5.6E-04 3
rs10497394 0.925 0.040 2 173432931 upstream gene variant C/T snv 0.23 2
rs766490137
NISCH
0.925 0.040 3 52458801 missense variant T/C snv 4.0E-06 2