Disease: Corpuscular Hemoglobin Concentration Mean
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 3
rs4082919
PGS1
17 78381401 intron variant T/G snv 0.55 2