Disease: Eosinophil count procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1036207
NDFIP1
1.000 0.080 5 142119476 intron variant A/G;T snv 3
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs113473633
NFKB1
1.000 0.040 4 102527974 intron variant A/G snv 1.6E-02 4
rs114269697
JAK1
1.000 0.040 1 64848529 intron variant C/A snv 7.3E-03 3
rs12935413
CLEC16A
1.000 0.080 16 11116590 intron variant G/A snv 0.34 2
rs2033784
SMAD3
1.000 0.080 15 67157322 intron variant A/G snv 0.35 3
rs2228467
CYP8B1 ; KRBOX1 ; ACKR2
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02 8
rs2248116
IRF1-AS1
1.000 0.040 5 132468655 intron variant C/A snv 0.70 2
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 3
rs3893464
HLA-A
1.000 0.120 6 29967473 downstream gene variant G/A snv 0.46 3
rs4760
PLAUR
1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 7
rs4807542
GPX4
1.000 0.120 19 1104079 synonymous variant G/A;C snv 0.22; 1.8E-05 3
rs56378716
MPO
1.000 0.080 17 58279141 missense variant A/G snv 1.0E-02 9.8E-03 5
rs61840192 1.000 0.080 10 9001441 intergenic variant G/A;C;T snv 3
rs8046011 1.000 0.120 16 11226805 downstream gene variant G/A;T snv 3
rs9504361
EXOC2
1.000 0.040 6 577820 intron variant A/G snv 0.40 3
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs2239630
CEBPE
0.925 0.160 14 23120140 upstream gene variant A/C;G snv 4
rs28383314 0.925 0.160 6 32619436 regulatory region variant T/C snv 0.61 4
rs301807
RERE-AS1 ; RERE
0.925 0.080 1 8424763 intron variant A/G;T snv 4
rs3755397
FARP2
0.925 0.120 2 241355498 upstream gene variant A/G snv 6.8E-02 4
rs3785356
IL4R
0.925 0.080 16 27337847 intron variant C/T snv 0.25 5
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 6
rs4821544
NCF4-AS1 ; NCF4
0.925 0.040 22 36862461 intron variant T/A;C snv 4