Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057520529
FOXP3
0.851 0.320 X 49251440 missense variant C/T snv 5
rs879253740
NPC2 ; ISCA2
0.882 0.240 14 74493191 splice donor variant A/G snv 5
rs587782477
APC
0.882 0.120 5 112775679 missense variant A/T snv 4
rs1217371203
CD86
0.882 0.120 3 122106342 missense variant A/G;T snv 4.0E-06; 4.0E-06 4
rs5743313
TLR3
0.851 0.200 4 186079213 intron variant C/T snv 0.19 4
rs868435969
VCP
0.925 0.280 9 35066710 missense variant G/A snv 3
rs4308977
CR2
0.925 0.160 1 207473553 missense variant T/A;C snv 4.0E-06; 0.27 2
rs17616
CR2
1.000 0.080 1 207473578 missense variant G/A snv 0.26 0.30 1