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
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs3130361 0.925 0.160 6 30371787 intergenic variant A/G snv 0.81 3
rs1419675 1.000 0.120 6 30124930 intergenic variant G/T snv 0.74 2
rs200968
H3C12 ; H2BC17
1.000 0.120 6 27891790 intron variant T/C snv 0.16 2
rs2107202
TRIM40
1.000 0.120 6 30137966 intron variant T/C snv 0.75 2