Disease: Eosinophil count procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10265538 7 20502242 intergenic variant T/C snv 0.20 2
rs10410864 19 39711776 downstream gene variant T/C snv 0.68 2
rs10542411 2 61541105 upstream gene variant ATATT/-;ATATTATATT delins 0.23 2
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
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs10893844 11 128315955 regulatory region variant G/C snv 0.36 2
rs111759324 1 101186966 upstream gene variant C/T snv 0.11 2
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs11359909 3 128603031 intergenic variant G/- delins 0.89 4
rs114050631 2 218156235 regulatory region variant C/T snv 6.9E-03 5
rs11725704 4 74094279 downstream gene variant A/G snv 0.28 5
rs11769630 7 50218107 intron variant T/A snv 5.4E-02 4
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs12542907 8 67900953 intergenic variant C/G snv 0.29 5
rs12600856 17 40007042 intergenic variant T/C;G snv 5
rs12752838 1 8853597 upstream gene variant A/G snv 0.54 4
rs12820863 12 4209557 intergenic variant C/T snv 0.27 2
rs13070844 3 12233786 intergenic variant G/A snv 0.25 2
rs13223928 7 3131386 intergenic variant T/C snv 0.51 2
rs138488218 12 53354069 regulatory region variant A/T snv 7.6E-03 4
rs16895831 6 42548053 regulatory region variant C/T snv 0.21 3
rs17005891 4 82626709 downstream gene variant G/A snv 0.15 3
rs175705 14 75509305 intergenic variant C/A;G;T snv 2
rs1912580 10 8995019 intergenic variant G/C snv 0.16 2