Disease: Eosinophil count procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10410864 19 39711776 downstream gene variant T/C snv 0.68 2
rs11725704 4 74094279 downstream gene variant A/G snv 0.28 5
rs149206763
LOC105371498
17 4618946 downstream gene variant G/A;C snv 2
rs17005891 4 82626709 downstream gene variant G/A snv 0.15 3
rs1991651
LOC101929248
8 10848901 downstream gene variant C/G snv 0.63 4
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs34762051 17 40007650 downstream gene variant AA/-;A;AAA delins 0.31 5
rs36229146 7 22744868 downstream gene variant AATATATATATATATATATATATATA/- delins 7.2E-02 2
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 6
rs3893464
HLA-A
1.000 0.120 6 29967473 downstream gene variant G/A snv 0.46 3
rs6803848 3 112138722 downstream gene variant G/A snv 5.0E-02 2
rs6986779 8 141327691 downstream gene variant C/T snv 0.34 4
rs71191701 9 136427805 downstream gene variant G/C;T snv 4
rs791357
LOC107986482
5 173778222 downstream gene variant T/A;C snv 4
rs8046011 1.000 0.120 16 11226805 downstream gene variant G/A;T snv 3
rs10542411 2 61541105 upstream gene variant ATATT/-;ATATTATATT delins 0.23 2
rs111759324 1 101186966 upstream gene variant C/T snv 0.11 2
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs12752838 1 8853597 upstream gene variant A/G snv 0.54 4
rs12968338
SERPINB13
18 63584740 upstream gene variant C/G;T snv 2
rs1968252
LOC105372263
19 7782850 upstream gene variant G/A;T snv 5
rs2029582
IL1RN
2 113106194 upstream gene variant T/C snv 0.56 4
rs2082382 5 148820990 upstream gene variant G/A snv 0.72 5
rs2239630
CEBPE
0.925 0.160 14 23120140 upstream gene variant A/C;G snv 4
rs2271400
LYN
8 55878685 upstream gene variant C/T snv 0.68 5