Disease: Eosinophil count procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10075801
MIR3936HG ; SLC22A4
5 132341949 intron variant A/G snv 0.31 5
rs10138752
RAD51B
14 68713254 intron variant C/T snv 8.8E-02 5
rs10165200
LINC00299
2 8299499 intron variant G/A snv 0.36 2
rs10173538
BAZ2B ; MARCHF7
2 159712765 intron variant C/G;T snv 5
rs10283564
INSL6 ; JAK2
9 5075628 intron variant C/G snv 0.23 2
rs1032726
CD200R1
3 112967228 intron variant T/C snv 0.46 2
rs1036207
NDFIP1
1.000 0.080 5 142119476 intron variant A/G;T snv 3
rs1036332
LINC01221
1 199043349 intron variant A/C snv 0.70 2
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs10852622
ZFPM1
16 88490472 intron variant A/G snv 0.35 2
rs10995240
LOC105378327 ; ZNF365
10 62628871 intron variant G/C snv 0.29 2
rs11127153
PLB1
2 28463094 intron variant T/A;C snv 2
rs111930700
ACVR1B
12 51967869 intron variant C/G snv 8.4E-02 4
rs11204682
ENSA
1 150623061 intron variant G/A;T snv 4
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
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