Disease: Corpuscular Hemoglobin Concentration Mean
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
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
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs10480300
PRKAG2
0.925 0.120 7 151708919 intron variant C/T snv 0.24 6
rs150551
CARMIL1
0.925 0.120 6 25533702 intron variant A/G;T snv 4
rs1028318
CARMIL1
0.925 0.120 6 25589996 intron variant T/C snv 0.27 4
rs2077393
CARMIL1
6 25607137 intron variant C/T snv 0.29 2
rs742132
CARMIL1
0.925 0.120 6 25607343 intron variant A/G snv 0.29 4
rs6903765
CARMIL1
0.925 0.120 6 25609510 intron variant A/G;T snv 4
rs6908390
CARMIL1
0.925 0.120 6 25609528 intron variant C/T snv 0.28 4
rs3804105
CARMIL1
0.925 0.120 6 25612455 intron variant A/C snv 0.29 4
rs10946785
CARMIL1
0.925 0.120 6 25616840 intron variant G/A;T snv 4
rs1997672
CARMIL1
0.925 0.120 6 25617316 intron variant T/G snv 0.28 4
rs7761700
CARMIL1
0.925 0.120 6 25617963 intron variant G/C;T snv 4
rs3757131
SLC17A1
0.882 0.200 6 25783681 intron variant C/T snv 0.32 5
rs13197601
SLC17A1
0.882 0.200 6 25785707 intron variant G/A snv 0.32 5
rs3799344
SLC17A1
0.882 0.200 6 25786765 intron variant C/T snv 0.41 5
rs2762353
SLC17A1
0.882 0.200 6 25794203 intron variant A/G snv 0.66 5
rs1165215
SLC17A1
0.882 0.200 6 25798704 3 prime UTR variant G/A snv 0.66 5
rs1165209
SLC17A1
0.925 0.120 6 25801091 intron variant G/A snv 0.66 4
rs1165196
SLC17A1
0.882 0.200 6 25812922 missense variant G/A snv 0.62 0.66 5
rs1165153
SLC17A1
0.925 0.120 6 25817561 intron variant A/G;T snv 4
rs1185567
SLC17A1
0.925 0.120 6 25818360 intron variant A/G;T snv 4