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
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 6
rs1800973
LYZ
0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 5
rs12459419
CD33
0.925 0.120 19 51225221 missense variant C/G;T snv 0.31 4
rs413141 19 6675978 downstream gene variant A/G snv 0.84 4
rs5112
APOC1P1
1.000 0.080 19 44927023 non coding transcript exon variant C/G snv 0.55 4
rs13207171
TREML2
6 41198081 intron variant C/T snv 0.12 0.10 2