Disease: Corpuscular Hemoglobin Concentration Mean
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
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
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 7
rs5762862
ZNRF3
22 28856744 intergenic variant G/A;T snv 4
rs12941884
SEZ6 ; PIPOX ; LOC105371716
17 28957425 missense variant A/G snv 0.15 0.16 2