Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7565639
PDCD1 ; LOC105373977
0.882 0.160 2 241854911 intron variant T/A;C snv 3
rs7519847
CELA3A
1.000 0.040 1 22003194 intron variant C/G;T snv 1
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs7421861
LOC105373977 ; PDCD1
0.790 0.200 2 241853198 intron variant A/G;T snv 9
rs703842
METTL1 ; CYP27B1
0.851 0.240 12 57768956 missense variant A/G snv 0.38 0.33 4
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs6841698 0.882 0.080 4 38760093 upstream gene variant G/A snv 0.36 4
rs6710479
LOC105373977 ; PDCD1
0.882 0.200 2 241855866 intron variant T/C snv 0.51 3
rs6703630
IL19
0.925 0.120 1 206775294 intron variant C/T snv 0.25 2
rs61860052
ANXA11
0.925 0.080 10 80201955 intron variant C/A snv 6.4E-02 2
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 6
rs4752
GC
1.000 0.040 4 71756849 synonymous variant A/G snv 3.8E-02 8.6E-02 1
rs4505848
KIAA1109
0.776 0.400 4 122211337 intron variant A/G snv 0.29 8
rs397514601
CAPN5
0.882 0.040 11 77115423 missense variant G/A;T snv 4.0E-06 3
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs377679652
GRB10
0.925 0.040 7 50669861 missense variant C/T snv 4.6E-05 2.8E-05 2
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2489188
TGFBR3
0.925 0.200 1 91866932 intron variant C/T snv 0.65 2
rs2358820
VTCN1
1.000 0.040 1 117169289 intron variant G/A snv 5.3E-02 1
rs2287987
ERAP1
0.882 0.120 5 96793832 missense variant T/C snv 0.15 0.16 3
rs2222202
IL10 ; IL19
0.827 0.160 1 206772036 intron variant G/A snv 0.39 5
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs2075800
HSPA1L
0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 8
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 14