Disease: Eosinophil count procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34332679 14 35412760 regulatory region variant -/A;AA delins 2
rs3831732
PTEN
10 87895485 intron variant -/A;AA delins 2
rs58548501 4 54635119 intergenic variant -/A;ATTTTTTTTTA ins 0.43 4
rs145013566
PNKD
2 218297998 intron variant -/C ins 5
rs540653847
HLA-B ; LOC112267902
6 31307016 intron variant -/C delins 4.2E-03 2
rs397933924 10 97314229 upstream gene variant -/CAGGTTCAAGCGA ins 5
rs776509440
KANSL1
17 46096136 intron variant -/CTT;CTTT;CTTTT;CTTTTT;CTTTTTT;CTTTTTTT;CTTTTTTTT;CTTTTTTTTTT;CTTTTTTTTTTTTTTT delins 2
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs11428934
CA11 ; SEC1P
19 48640988 intron variant -/G ins 4
rs5833013
IL1RL1 ; IL18R1
2 102352407 intron variant -/TA delins 2
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs11319879
HHEX
10 92693719 intron variant A/- delins 0.53 2
rs75802552
IL21-AS1
4 122678167 intron variant A/- delins 0.35 2
rs1036332
LINC01221
1 199043349 intron variant A/C snv 0.70 2
rs11654074
VMP1
17 59748211 intron variant A/C snv 0.40 5
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs147453535
CEBPE
14 23117837 intron variant A/C snv 6.3E-03 6.2E-03 2
rs2072735
SPSB1
1 9295413 intron variant A/C snv 0.76 2
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs2239630
CEBPE
0.925 0.160 14 23120140 upstream gene variant A/C;G snv 4
rs7288670
GGT5
22 24225858 intron variant A/C;G snv 4
rs10075801
MIR3936HG ; SLC22A4
5 132341949 intron variant A/G snv 0.31 5
rs10852622
ZFPM1
16 88490472 intron variant A/G snv 0.35 2
rs113473633
NFKB1
1.000 0.040 4 102527974 intron variant A/G snv 1.6E-02 4
rs11725704 4 74094279 downstream gene variant A/G snv 0.28 5