Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs3129871
HLA-DRA
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs7185022
IRF8
1.000 0.120 16 85919323 intron variant A/C snv 0.63 1
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs2227981
LOC105373977 ; PDCD1
0.763 0.400 2 241851121 synonymous variant A/C;G snv 1.6E-04; 0.63 12
rs1382568
BLK
0.925 0.160 8 11493711 intron variant A/C;G snv 2
rs2857151 0.925 0.160 6 32795737 intergenic variant A/C;G snv 2
rs7305115
TPH2
0.807 0.200 12 71979082 synonymous variant A/C;G;T snv 4.0E-06; 0.56 8
rs2618458
BLK
1.000 0.120 8 11511559 intron variant A/C;G;T snv 1
rs2736335 1.000 0.120 8 11483978 upstream gene variant A/C;G;T snv 1
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs2618444 0.925 0.160 8 11480861 intron variant A/C;T snv 2
rs2736338 1.000 0.120 8 11484374 upstream gene variant A/C;T snv 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs57095329
MIR3142HG
0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs4523
TBXA2R
0.776 0.280 19 3595796 missense variant A/G snv 0.56 0.66 8
rs6906846
HLA-B ; USP8P1
0.851 0.280 6 31277959 non coding transcript exon variant A/G snv 0.67 7
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 6
rs707928
VWA7
0.827 0.320 6 31774813 intron variant A/G snv 0.47 5
rs12901071
SMAD3
0.882 0.160 15 67078051 intron variant A/G snv 0.25 3
rs2736345
BLK
0.882 0.280 8 11494976 intron variant A/G snv 0.35 3
rs12900413
MESP2
0.925 0.120 15 89777808 intron variant A/G snv 0.27 2
rs2618479
BLK
0.925 0.280 8 11498312 intron variant A/G snv 0.84 2
rs1150793
MSH5 ; MSH5-SAPCD1
1.000 0.120 6 31749919 intron variant A/G snv 0.11 1
rs17416878 1.000 0.120 1 16120485 downstream gene variant A/G snv 0.24 1