Disease: White Blood Cell Count procedure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10206089 2 61476184 intron variant G/A snv 4
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
rs12542907 8 67900953 intergenic variant C/G snv 0.29 5
rs12600856 17 40007042 intergenic variant T/C;G snv 5
rs13138355 4 82624823 upstream gene variant C/A;T snv 4
rs143699489 3 141208279 intergenic variant A/G snv 0.22 4
rs1449263 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 5
rs17005891 4 82626709 downstream gene variant G/A snv 0.15 3
rs200638392 6 87128241 intergenic variant GAT/-;GATGAT delins 0.47 5
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 10
rs2338224 5 72432861 intergenic variant A/G snv 0.85 5
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs34293785 1 65671509 intergenic variant T/C snv 4
rs34762051 17 40007650 downstream gene variant AA/-;A;AAA delins 0.31 5
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 9
rs397933924 10 97314229 upstream gene variant -/CAGGTTCAAGCGA ins 5
rs4328821 3 128597592 intergenic variant A/G snv 0.13 3
rs4794822 17 40000459 downstream gene variant C/G;T snv 3
rs60606273 15 64362768 intron variant A/T snv 0.84 5
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8