Disease: Eosinophil count procedure
Source: GWASCAT ×
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 34
rs11359909 3 128603031 intergenic variant G/- delins 0.89 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
rs1586068
IKZF2
2 213033508 intron variant A/G snv 0.81 2
rs301161
EMC8
16 85776743 intron variant G/A snv 0.81 2
rs7613595
PLCL2
3 16867007 intron variant C/A snv 0.79 2
rs2072735
SPSB1
1 9295413 intron variant A/C snv 0.76 2
rs4848100
ANAPC1
2 111630955 non coding transcript exon variant C/T snv 0.76 2
rs2335455
ELOB
16 2778172 non coding transcript exon variant T/C;G snv 0.74 2
rs511515
GGNBP1 ; BAK1
6 33573730 3 prime UTR variant A/G snv 0.73 2
rs2998286
LINC02652
10 28491444 intron variant T/C snv 0.73 5
rs2082382 5 148820990 upstream gene variant G/A snv 0.72 5
rs4449834
CHD7
8 60843309 intron variant G/T snv 0.71 2
rs1036332
LINC01221
1 199043349 intron variant A/C snv 0.70 2
rs2248116
IRF1-AS1
1.000 0.040 5 132468655 intron variant C/A snv 0.70 2
rs2158799
JAZF1-AS1
7 28237488 intron variant C/G;T snv 0.70 5
rs2271400
LYN
8 55878685 upstream gene variant C/T snv 0.68 5
rs10410864 19 39711776 downstream gene variant T/C snv 0.68 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 3