Disease: Corpuscular Hemoglobin Concentration Mean
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs807212 0.925 0.120 6 26065393 regulatory region variant A/G;T snv 5
rs942379
SLC17A3
0.925 0.120 6 25849392 missense variant A/G;T snv 0.60 4
rs1183201
SLC17A1
0.925 0.120 6 25823216 intron variant A/T snv 0.65 4
rs9467664
H4C1
0.925 0.120 6 26021585 upstream gene variant A/T snv 0.76 5
rs6905614
SLC17A3
0.925 0.120 6 25840257 intron variant C/A;G snv 4
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs10480300
PRKAG2
0.925 0.120 7 151708919 intron variant C/T snv 0.24 6
rs199736 0.925 0.120 6 25936559 intergenic variant C/T snv 0.72 5
rs199750 0.882 0.160 6 26016234 upstream gene variant C/T snv 0.77 5
rs199752 0.925 0.120 6 26012647 upstream gene variant C/T snv 0.77 5
rs2077393
CARMIL1
6 25607137 intron variant C/T snv 0.29 2
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
rs3799352
SLC17A1
0.925 0.120 6 25822392 intron variant C/T snv 0.65 4
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs6908390
CARMIL1
0.925 0.120 6 25609528 intron variant C/T snv 0.28 4
rs1165196
SLC17A1
0.882 0.200 6 25812922 missense variant G/A snv 0.62 0.66 5
rs1165209
SLC17A1
0.925 0.120 6 25801091 intron variant G/A snv 0.66 4
rs1165215
SLC17A1
0.882 0.200 6 25798704 3 prime UTR variant G/A snv 0.66 5
rs13197601
SLC17A1
0.882 0.200 6 25785707 intron variant G/A snv 0.32 5
rs199726 0.925 0.120 6 25953132 intergenic variant G/A snv 0.73 5
rs199753 0.925 0.120 6 26001660 non coding transcript exon variant G/A snv 0.77 5
rs2213284
H3C2
0.925 0.120 6 26031640 3 prime UTR variant G/A snv 0.70 0.76 4
rs2230655
H2AC4 ; H3C2
0.882 0.160 6 26033278 synonymous variant G/A snv 0.71 0.76 5
rs4401650
H2AC4
0.925 0.120 6 26034980 upstream gene variant G/A snv 0.75 5