Disease: Corpuscular Hemoglobin Concentration Mean
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199750 0.882 0.160 6 26016234 upstream gene variant C/T snv 0.77 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
rs2230655
H2AC4 ; H3C2
0.882 0.160 6 26033278 synonymous variant G/A snv 0.71 0.76 5
rs2762353
SLC17A1
0.882 0.200 6 25794203 intron variant A/G snv 0.66 5
rs35385468 0.925 0.120 6 26101212 upstream gene variant -/C delins 9.7E-03 5
rs3757131
SLC17A1
0.882 0.200 6 25783681 intron variant C/T snv 0.32 5
rs3799344
SLC17A1
0.882 0.200 6 25786765 intron variant C/T snv 0.41 5
rs386406569 0.925 0.120 6 26101212 upstream gene variant -/C delins 5
rs4401650
H2AC4
0.925 0.120 6 26034980 upstream gene variant G/A snv 0.75 5
rs442601 0.925 0.120 6 25934296 upstream gene variant G/A snv 0.72 5
rs744103
LOC105375069 ; LOC107986598
0.925 0.120 6 43837625 intron variant T/A snv 0.58 5
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
rs9467664
H4C1
0.925 0.120 6 26021585 upstream gene variant A/T snv 0.76 5
rs1028318
CARMIL1
0.925 0.120 6 25589996 intron variant T/C snv 0.27 4
rs10425
H1-2
0.925 0.120 6 26056321 synonymous variant A/G snv 0.68 0.73 4
rs10946785
CARMIL1
0.925 0.120 6 25616840 intron variant G/A;T snv 4
rs1165151
SLC17A1
0.925 0.120 6 25821388 intron variant T/A;G snv 4
rs1165152
SLC17A1
0.925 0.120 6 25818538 intron variant A/C;G;T snv 4
rs1165153
SLC17A1
0.925 0.120 6 25817561 intron variant A/G;T snv 4
rs1165160
SLC17A3
0.925 0.120 6 25864228 intron variant A/G snv 0.64 4
rs1165176
SLC17A1
0.925 0.120 6 25830070 intron variant A/G snv 0.65 4
rs1165177
SLC17A1
0.925 0.120 6 25829431 intron variant T/A snv 0.65 4