Disease: Corpuscular Hemoglobin Concentration Mean
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs942379
SLC17A3
0.925 0.120 6 25849392 missense variant A/G;T snv 0.60 4
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs35385468 0.925 0.120 6 26101212 upstream gene variant -/C delins 9.7E-03 5
rs2834319
LOC105372790
21 33984724 regulatory region variant T/C snv 0.16 2
rs10480300
PRKAG2
0.925 0.120 7 151708919 intron variant C/T snv 0.24 6
rs1028318
CARMIL1
0.925 0.120 6 25589996 intron variant T/C snv 0.27 4
rs198853
H4C3
0.925 0.120 6 26103868 upstream gene variant T/C snv 0.28 5
rs1997672
CARMIL1
0.925 0.120 6 25617316 intron variant T/G snv 0.28 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
rs742132
CARMIL1
0.925 0.120 6 25607343 intron variant A/G snv 0.29 4
rs2077393
CARMIL1
6 25607137 intron variant C/T snv 0.29 2
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs13197601
SLC17A1
0.882 0.200 6 25785707 intron variant G/A snv 0.32 5
rs3757131
SLC17A1
0.882 0.200 6 25783681 intron variant C/T snv 0.32 5
rs7209801 17 44246008 downstream gene variant G/A snv 0.38 2
rs3799344
SLC17A1
0.882 0.200 6 25786765 intron variant C/T snv 0.41 5
rs9393676 0.925 0.120 6 25936716 intergenic variant G/A snv 0.45 4
rs9295678 0.925 0.120 6 25936805 intergenic variant G/A snv 0.45 4
rs2051541 0.925 0.120 6 25944983 regulatory region variant A/G snv 0.47 4
rs9379801 0.925 0.120 6 25901483 intergenic variant T/C snv 0.48 4
rs9393672
SLC17A3
0.925 0.120 6 25842377 intron variant T/G snv 0.51 4
rs744103
LOC105375069 ; LOC107986598
0.925 0.120 6 43837625 intron variant T/A snv 0.58 5
rs1165160
SLC17A3
0.925 0.120 6 25864228 intron variant A/G snv 0.64 4
rs1165207
SLC17A3
0.925 0.120 6 25865038 intron variant T/C snv 0.64 4