Disease: White Blood Cell Count procedure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
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
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 21
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs174549
FADS2 ; FADS1
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 12
rs61754230
RAB21
12 71785666 missense variant C/T snv 1.3E-02 1.2E-02 4
rs56204645
RP1
8 54509209 upstream gene variant T/C snv 0.19 3