Disease: Finding of Mean Corpuscular Hemoglobin
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12216125 0.925 0.120 6 25997230 intron variant C/T snv 0.26 6
rs3887266
SLC17A3
0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02 6
rs2794719
LOC108783645 ; HFE
0.925 0.120 6 26088662 intron variant T/C;G snv 5
rs9295684 0.925 0.120 6 26069441 intergenic variant T/C snv 0.38 5
rs9379818 0.925 0.120 6 26022978 downstream gene variant G/A;T snv 5