Disease: Red Blood Cell Count measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs1150660 0.925 0.120 6 26101212 upstream gene variant A/C snv 0.73 5
rs199726 0.925 0.120 6 25953132 intergenic variant G/A snv 0.73 5
rs199734 0.925 0.120 6 25940165 intergenic variant G/A;C snv 5
rs199736 0.925 0.120 6 25936559 intergenic variant C/T snv 0.72 5
rs199737 0.925 0.120 6 25933310 upstream gene variant A/C;T snv 5
rs199739 0.925 0.120 6 25960281 upstream gene variant A/C;G snv 0.78 5
rs199751 0.925 0.120 6 26015355 upstream gene variant T/C snv 0.77 5
rs199752 0.925 0.120 6 26012647 upstream gene variant C/T snv 0.77 5
rs199753 0.925 0.120 6 26001660 non coding transcript exon variant G/A snv 0.77 5
rs35385468 0.925 0.120 6 26101212 upstream gene variant -/C delins 9.7E-03 5
rs386406569 0.925 0.120 6 26101212 upstream gene variant -/C delins 5
rs442601 0.925 0.120 6 25934296 upstream gene variant G/A snv 0.72 5
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs807212 0.925 0.120 6 26065393 regulatory region variant A/G;T snv 5
rs9358901 0.925 0.120 6 26024208 downstream gene variant G/T snv 0.67 5
rs12987661
AAK1
2 69586326 intron variant T/C snv 0.11 2
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 10
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs4401650
H2AC4
0.925 0.120 6 26034980 upstream gene variant G/A snv 0.75 5
rs7756117
H3C3
0.882 0.160 6 26046337 upstream gene variant G/A snv 0.69 6
rs2032447
H3C3 ; H2BC3 ; H2AC5P
0.925 0.120 6 26044141 non coding transcript exon variant A/G snv 4.1E-06; 0.67 0.67 6