Disease: Neutrophil count (procedure)
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs174555
FADS2 ; FADS1
11 61812288 intron variant T/C snv 0.26 4
rs61897795
FADS2
11 61850697 intron variant A/G snv 9.5E-02 3