Disease: Eosinophil count procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1754541
LOC101928334
1 101160327 intergenic variant A/G snv 0.25 2
rs7168592
CHSY1
15 101183294 intron variant C/T snv 9.8E-02 4
rs111759324 1 101186966 upstream gene variant C/T snv 0.11 2
rs114743735
IRAK2
3 10186296 intron variant C/G snv 4.2E-02 2
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs5833013
IL1RL1 ; IL18R1
2 102352407 intron variant -/TA delins 2
rs34020101
IL18RAP
2 102435015 non coding transcript exon variant AA/-;A;AAA delins 2
rs113473633
NFKB1
1.000 0.040 4 102527974 intron variant A/G snv 1.6E-02 4
rs113422568
SUFU
10 102578181 intron variant G/A snv 0.25 2
rs2436845
AZIN1
8 102840179 intron variant G/A snv 0.37 4
rs4147915
ABCA7
19 1049306 synonymous variant C/A;G snv 0.18; 4.0E-06 3
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 23
rs3822411
DAP
5 10684830 intron variant T/C snv 0.42 2
rs6568466 6 107122949 intergenic variant T/C snv 0.58 2
rs36084354
ARHGAP45
19 1079960 missense variant G/A snv 5.7E-02 5.9E-02 3
rs663045
SLC25A24
1 108200437 5 prime UTR variant G/C snv 0.55 5
rs582297
ATM
11 108294680 intron variant C/A;G snv 2
rs192022
C11orf65
11 108378047 intron variant C/G;T snv 5
rs1991651
LOC101929248
8 10848901 downstream gene variant C/G snv 0.63 4
rs9400271
CCDC162P
6 109286353 non coding transcript exon variant G/A snv 0.51 5
rs4807542
GPX4
1.000 0.120 19 1104079 synonymous variant G/A;C snv 0.22; 1.8E-05 3
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs551517
LPAR1
9 110874513 3 prime UTR variant C/T snv 0.27 2
rs55905691
WDR36
5 111090287 intron variant A/G snv 0.13 2
rs79881201
WDR36
5 111092097 5 prime UTR variant C/T snv 0.26 2