Disease: Corpuscular Hemoglobin Concentration Mean
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs10480300
PRKAG2
0.925 0.120 7 151708919 intron variant C/T snv 0.24 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
rs4886755
NRG4
0.925 0.120 15 76005791 non coding transcript exon variant A/G;T snv 0.49 6
rs729761
LOC105375069 ; LOC107986598
0.925 0.120 6 43836834 intron variant T/A;G snv 6
rs7756117
H3C3
0.882 0.160 6 26046337 upstream gene variant G/A snv 0.69 6
rs1150660 0.925 0.120 6 26101212 upstream gene variant A/C snv 0.73 5
rs115810
TRIM38
0.925 0.120 6 25975655 intron variant G/A;C snv 5
rs1165196
SLC17A1
0.882 0.200 6 25812922 missense variant G/A snv 0.62 0.66 5
rs1165215
SLC17A1
0.882 0.200 6 25798704 3 prime UTR variant G/A snv 0.66 5
rs129129
TRIM38
0.925 0.120 6 25960801 upstream gene variant A/G snv 0.73 5
rs13197601
SLC17A1
0.882 0.200 6 25785707 intron variant G/A snv 0.32 5
rs1540276
H4C2
0.925 0.120 6 26028591 upstream gene variant T/A;G snv 5
rs198853
H4C3
0.925 0.120 6 26103868 upstream gene variant T/C snv 0.28 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