Disease: Eosinophil count procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs2228467
CYP8B1 ; KRBOX1 ; ACKR2
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02 8
rs2954031 8 125479491 intron variant G/T snv 0.42 8
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs9532434
COG6
0.807 0.120 13 39781776 intron variant T/A;C snv 8
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 7
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26 7
rs143034248
JAML
11 118210555 missense variant C/T snv 4.0E-03 3.5E-03 7
rs2038700
STXBP6
14 24992783 intron variant T/C snv 0.53 7
rs34599082
ACKR1 ; CADM3-AS1
1 159205704 missense variant C/T snv 1.1E-02 9.9E-03 7
rs4760
PLAUR
1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 7
rs6782228 3 128604581 intergenic variant G/C snv 0.28 7
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24 7
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 6
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs2524079
HLA-B
6 31274397 intron variant G/A snv 0.44 6
rs2979489
RBPMS
8 30423317 intron variant G/A;C snv 6
rs34208856
HBS1L
6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins 6
rs3735485
MYO1G
7 44969742 missense variant A/G snv 0.87 0.88 6
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 6
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs9271588 0.925 0.200 6 32623176 TF binding site variant T/C snv 0.43 6