Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs661561
TNFAIP3
0.882 0.200 6 137876194 intron variant A/C snv 0.62 0.50 3
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs17855750
IL27
0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 21
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs7629750
TMEM39A
0.882 0.040 3 119455829 intron variant A/G snv 0.45 3
rs853326
TG
0.882 0.120 8 132897729 missense variant A/G snv 0.58 0.60 3
rs2048722
TPO
0.925 2 1492028 intron variant A/G snv 0.51 2
rs2227478
IL22 ; LOC105369818
0.925 0.040 12 68254842 upstream gene variant A/G snv 0.37 2
rs2618431
FAM167A
0.925 0.120 8 11466955 intron variant A/G snv 0.87 2
rs2292399
PPDPFL
1.000 8 49074671 3 prime UTR variant A/G snv 0.31 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs689
INS ; INS-IGF2
0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60 9
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs3788013
UBASH3A
0.851 0.240 21 42421219 intron variant C/A snv 0.44 5
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2276886
CXCL9
0.882 0.120 4 76007275 intron variant C/A;T snv 3
rs1179251
IL22 ; LOC105369818
0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs17593222
STAT3
0.925 0.120 17 42360972 intron variant C/G snv 6.1E-02 3
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 19
rs28665122
SELENOS
0.807 0.240 15 101277522 upstream gene variant C/T snv 0.24 7
rs2076740
TG
0.827 0.160 8 132971813 missense variant C/T snv 0.31 0.37 5
rs12492609
TMEM39A
0.882 0.040 3 119435715 intron variant C/T snv 0.14 3