Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs765613977
AAAS
0.882 0.080 12 53321465 start lost T/C snv 4.0E-06 7.0E-06 3
rs2237025
KIT
0.882 0.080 4 54675713 intron variant T/C snv 0.60 3
rs6554199
KIT
0.925 0.040 4 54656321 upstream gene variant G/T snv 0.54 2