Disease: Eosinophil count procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs68191221
KLF3
4 38675441 intron variant A/G snv 0.18 2
rs73036517
MARK4 ; EXOC3L2
19 45241584 intron variant A/G snv 0.20 4
rs77972791
ELMO1
7 37364044 intron variant A/G snv 8.2E-02 2
rs7834745
TNFRSF11B
8 118927620 intron variant A/G snv 0.18 2
rs834603
TNS3
7 47408324 intron variant A/G snv 0.47 4
rs9504361
EXOC2
1.000 0.040 6 577820 intron variant A/G snv 0.40 3
rs1036207
NDFIP1
1.000 0.080 5 142119476 intron variant A/G;T snv 3
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs2834081
LINC00945
21 33060486 intron variant A/G;T snv 2
rs2856451
TNXB
6 32043581 intron variant A/G;T snv 0.59 3
rs301807
RERE-AS1 ; RERE
0.925 0.080 1 8424763 intron variant A/G;T snv 4
rs45577137
CEBPD
8 47739071 upstream gene variant A/G;T snv 4
rs7141943
STXBP6
14 24969044 intron variant A/G;T snv 3
rs960709
TNIP1
0.882 0.120 5 151081488 intron variant A/G;T snv 4
rs11669910
EXOC3L2 ; MARK4
19 45238075 intron variant A/T snv 0.23 2
rs13007211
VAMP8
2 85573959 intron variant A/T snv 0.31 2
rs138488218 12 53354069 regulatory region variant A/T snv 7.6E-03 4
rs42033
CDK6
0.882 0.080 7 92608219 3 prime UTR variant A/T snv 0.16 2
rs60606273 15 64362768 intron variant A/T snv 0.84 5
rs62264129
CD200
3 112352566 intron variant A/T snv 0.27 2
rs6684992 1 87286317 intergenic variant A/T snv 0.20 2
rs675600
LINC02210 ; LINC02210-CRHR1
17 45618793 upstream gene variant A/T snv 0.14 4
rs7846314
CHD7
8 60738272 intron variant A/T snv 0.27 5
rs34020101
IL18RAP
2 102435015 non coding transcript exon variant AA/-;A;AAA delins 2