Disease: Lymphocyte Count measurement
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
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs2524079
HLA-B
6 31274397 intron variant G/A snv 0.44 6
rs3735485
MYO1G
7 44969742 missense variant A/G snv 0.87 0.88 6
rs13063578
SETD2
3 47046347 intron variant T/A snv 0.46 5
rs36084354
ARHGAP45
19 1079960 missense variant G/A snv 5.7E-02 5.9E-02 3
rs3131643
HCP5
6 31475005 intron variant G/A snv 0.12 2