Disease: White Blood Cell 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
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 7
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 6
rs138682554
FES
15 90884462 5 prime UTR variant G/A snv 1.5E-02 2
rs144317085 4 104884951 intron variant A/T snv 2.6E-02 2
rs55714120
PHB
17 49411461 intron variant G/T snv 0.24 2
rs758374
ARVCF
22 19984029 intron variant T/C snv 0.27 2