Disease: Eosinophil count procedure
Source: GWASCAT ×
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 61
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs3895874
GIP
1.000 0.040 17 48970506 upstream gene variant G/A;C snv 2