Disease: Eosinophil count procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 8
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 6
rs16903574
OTULINL
0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 6
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs1444782 0.851 0.240 10 9016708 intergenic variant G/A snv 0.35 5
rs3785356
IL4R
0.925 0.080 16 27337847 intron variant C/T snv 0.25 5
rs55646091 0.925 0.080 11 76588387 upstream gene variant G/A snv 3.0E-02 5
rs7936312 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 5
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs11071559
RORA
0.925 0.080 15 60777789 intron variant C/T snv 0.23 4
rs12722502
IL2RA
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 4
rs3024971
STAT6
0.827 0.200 12 57099944 intron variant T/G snv 7.8E-02 7.9E-02 4
rs61894547
EMSY
0.882 0.160 11 76537586 intron variant C/T snv 3.1E-02 4
rs10905284
GATA3
0.882 0.200 10 8073399 intron variant C/A;T snv 3
rs12952581
LOC102724596
0.925 0.080 17 49370984 intron variant G/A snv 0.42 0.28 3
rs1420101
IL1RL1 ; IL18R1
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 3
rs2033784
SMAD3
1.000 0.080 15 67157322 intron variant A/G snv 0.35 3
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 3
rs61840192 1.000 0.080 10 9001441 intergenic variant G/A;C;T snv 3