Disease: Neutrophil count (procedure)
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs11137087 8 7048518 intergenic variant A/G snv 0.60 2
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
rs13187922 5 142083096 intergenic variant C/T snv 0.48 3
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
rs1999537 1 56439852 intron variant G/A snv 0.89 2
rs200638392 6 87128241 intergenic variant GAT/-;GATGAT delins 0.47 5
rs201399927 2 24377011 intergenic variant TT/-;T;TTT;TTTT delins 0.18 2
rs201950044 1 161639782 intergenic variant G/T snv 5
rs2082382 5 148820990 upstream gene variant G/A snv 0.72 5
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs2251188 7 6664701 intron variant A/G snv 0.71 2
rs2338224 5 72432861 intergenic variant A/G snv 0.85 5
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs2954031 8 125479491 intron variant G/T snv 0.42 8
rs34293785 1 65671509 intergenic variant T/C snv 4
rs34762051 17 40007650 downstream gene variant AA/-;A;AAA delins 0.31 5