Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 8
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs1061502
IRF7
0.882 0.160 11 614318 missense variant T/C snv 0.25 0.33 3
rs1131665
IRF7
0.851 0.160 11 613208 missense variant T/C snv 0.25 0.33 4
rs1179251
IL22 ; LOC105369818
0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs12492609
TMEM39A
0.882 0.040 3 119435715 intron variant C/T snv 0.14 3
rs1267634673
THRB
0.925 0.040 3 24127628 missense variant C/T snv 2
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs17445836 0.851 0.320 16 85984057 intron variant G/A snv 0.15 5
rs17593222
STAT3
0.925 0.120 17 42360972 intron variant C/G snv 6.1E-02 3
rs17855750
IL27
0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 21
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2048722
TPO
0.925 2 1492028 intron variant A/G snv 0.51 2
rs2069550
TG
0.925 0.120 8 132888141 synonymous variant T/C snv 0.58 0.60 2
rs2071400
TPO
0.882 0.120 2 1412867 intron variant C/T snv 0.11 3
rs2076740
TG
0.827 0.160 8 132971813 missense variant C/T snv 0.31 0.37 5
rs2227478
IL22 ; LOC105369818
0.925 0.040 12 68254842 upstream gene variant A/G snv 0.37 2
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2276886
CXCL9
0.882 0.120 4 76007275 intron variant C/A;T snv 3
rs2280381 0.882 0.080 16 85985027 intron variant C/T snv 0.64 3
rs2292399
PPDPFL
1.000 8 49074671 3 prime UTR variant A/G snv 0.31 1