Disease: Eosinophil count procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs11319879
HHEX
10 92693719 intron variant A/- delins 0.53 2
rs11327184
CCDC26
8 129592027 intron variant C/- delins 0.40 4
rs113422568
SUFU
10 102578181 intron variant G/A snv 0.25 2
rs113473633
NFKB1
1.000 0.040 4 102527974 intron variant A/G snv 1.6E-02 4
rs11353326
ARIH2
3 48941172 intron variant AAAAA/-;A;AA;AAA;AAAA;AAAAAA;AAAAAAA delins 2
rs11359909 3 128603031 intergenic variant G/- delins 0.89 4
rs114050631 2 218156235 regulatory region variant C/T snv 6.9E-03 5
rs114269697
JAK1
1.000 0.040 1 64848529 intron variant C/A snv 7.3E-03 3
rs11428934
CA11 ; SEC1P
19 48640988 intron variant -/G ins 4
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv 5
rs11465296
CCL24
7 75812976 intron variant C/T snv 4.9E-02 2
rs114743735
IRAK2
3 10186296 intron variant C/G snv 4.2E-02 2
rs11624512
RIN3
14 92644775 non coding transcript exon variant C/T snv 0.15 5
rs11654074
VMP1
17 59748211 intron variant A/C snv 0.40 5
rs11669910
EXOC3L2 ; MARK4
19 45238075 intron variant A/T snv 0.23 2
rs11725704 4 74094279 downstream gene variant A/G snv 0.28 5
rs11734460
PCGF3
4 711285 intron variant C/A;T snv 4
rs11769630 7 50218107 intron variant T/A snv 5.4E-02 4
rs11786130
PVT1
8 127992729 intron variant G/A snv 0.31 2
rs117868203
GFI1B
9 132982259 intron variant C/T snv 1.1E-02 2
rs11931598
LOC100129931 ; TADA2B
4 7045375 intron variant C/T snv 0.55 4
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 7
rs12264390
LARP4B
10 913171 intron variant T/C snv 0.20 2
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26 7