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
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs5742909
CTLA4
0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs237025
SUMO4 ; TAB2
0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs689
INS ; INS-IGF2
0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60 9
rs7961581
TSPAN8
0.827 0.200 12 71269322 intron variant C/T snv 0.75 7
rs3957146 0.882 0.200 6 32713753 upstream gene variant T/C snv 9.1E-02 3
rs231806 0.925 0.120 2 203844626 intergenic variant C/G;T snv 2
rs12571751
ZMIZ1
0.925 0.120 10 79182874 intron variant A/G snv 0.46 2