Disease: Eosinophil count procedure
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
rs7537229 1 56440602 intron variant G/A snv 0.92 4
rs3735485
MYO1G
7 44969742 missense variant A/G snv 0.87 0.88 6
rs2338224 5 72432861 intergenic variant A/G snv 0.85 5
rs60606273 15 64362768 intron variant A/T snv 0.84 5
rs12550612
TNFRSF10C
8 23109256 intron variant G/A snv 0.83 5
rs2998286
LINC02652
10 28491444 intron variant T/C snv 0.73 5
rs2082382 5 148820990 upstream gene variant G/A snv 0.72 5
rs2158799
JAZF1-AS1
7 28237488 intron variant C/G;T snv 0.70 5
rs7575217
TBC1D8
2 101160470 intron variant A/G snv 0.68 3
rs2271400
LYN
8 55878685 upstream gene variant C/T snv 0.68 5
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1991651
LOC101929248
8 10848901 downstream gene variant C/G snv 0.63 4
rs9287604 2 236867522 intergenic variant G/C snv 0.62 5
rs1025687
MAPK4
18 50621423 intron variant T/C snv 0.61 3
rs3917932
CSF3R
1 36478315 intron variant C/G snv 0.59 5
rs1570884
RCBTB1
13 49547375 intron variant A/G snv 0.58 4
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 9
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs9436747
LEPR
1 65445924 intron variant T/C snv 0.56 5
rs2029582
IL1RN
2 113106194 upstream gene variant T/C snv 0.56 4
rs663045
SLC25A24
1 108200437 5 prime UTR variant G/C snv 0.55 5
rs11931598
LOC100129931 ; TADA2B
4 7045375 intron variant C/T snv 0.55 4
rs12752838 1 8853597 upstream gene variant A/G snv 0.54 4