Disease: Eosinophil count procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9979383
RUNX1
0.925 0.200 21 35343463 intron variant C/G;T snv 5
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs9917425
OTOR
20 16755400 intron variant G/T snv 0.16 13
rs9900933
UNK
17 75805073 intron variant T/A;C;G snv 3
rs9872570
KRBOX1 ; ACKR2
3 42855023 intron variant T/A snv 0.37 3
rs9829778
PAK2
3 196822218 intron variant G/A snv 0.53 2
rs9819371
RASA2
3 141487958 intron variant C/T snv 4.7E-02 5
rs9811216
ACTRT3
3 169769713 non coding transcript exon variant T/C snv 0.29 2
rs960709
TNIP1
0.882 0.120 5 151081488 intron variant A/G;T snv 4
rs9532434
COG6
0.807 0.120 13 39781776 intron variant T/A;C snv 8
rs9504361
EXOC2
1.000 0.040 6 577820 intron variant A/G snv 0.40 3
rs9436747
LEPR
1 65445924 intron variant T/C snv 0.56 5
rs9402682
HBS1L
6 135085045 intron variant G/T snv 0.42 2
rs9400271
CCDC162P
6 109286353 non coding transcript exon variant G/A snv 0.51 5
rs9287604 2 236867522 intergenic variant G/C snv 0.62 5
rs9271588 0.925 0.200 6 32623176 TF binding site variant T/C snv 0.43 6
rs9266428 6 31369434 intron variant G/A snv 0.22 2
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24 7
rs8705
ETS1
11 128459018 3 prime UTR variant G/A;T snv 5
rs834603
TNS3
7 47408324 intron variant A/G snv 0.47 4
rs8179
CDK6
0.882 0.080 7 92606850 3 prime UTR variant T/A;C;G snv 5
rs8176685
ABO
9 133263363 intron variant CACCACTACGCC/- delins 4
rs8133974
RUNX1
21 35078544 intron variant C/T snv 0.11 3
rs8046011 1.000 0.120 16 11226805 downstream gene variant G/A;T snv 3
rs8
CDK6
7 92779015 intron variant C/T snv 0.14 2