Disease: Eosinophil count procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17484848
BCL2L11 ; MIR4435-2HG
2 111142983 intron variant T/C snv 7.2E-02 2
rs12935413
CLEC16A
1.000 0.080 16 11116590 intron variant G/A snv 0.34 2
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs4848100
ANAPC1
2 111630955 non coding transcript exon variant C/T snv 0.76 2
rs6803848 3 112138722 downstream gene variant G/A snv 5.0E-02 2
rs555346412
HECTD4
12 112191863 intron variant G/C snv 8.2E-04 5
rs8046011 1.000 0.120 16 11226805 downstream gene variant G/A;T snv 3
rs62264129
CD200
3 112352566 intron variant A/T snv 0.27 2
rs1032726
CD200R1
3 112967228 intron variant T/C snv 0.46 2
rs2029582
IL1RN
2 113106194 upstream gene variant T/C snv 0.56 4
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs2846630
ZBTB16
11 114086475 intron variant G/A snv 0.35 5
rs238914
ZBTB16
11 114113387 intron variant C/A snv 0.45 5
rs3181348
TNFSF8 ; DELEC1
9 114931904 intron variant G/A;C snv 2
rs66505542
BUD13
11 116752498 intron variant AA/-;A;AAA delins 5
rs77204473
SIK3
11 116934348 intron variant T/C;G snv 2
rs143034248
JAML
11 118210555 missense variant C/T snv 4.0E-03 3.5E-03 7
rs7834745
TNFRSF11B
8 118927620 intron variant A/G snv 0.18 2
rs35249183 1 12039288 upstream gene variant A/G snv 6.4E-02 2
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
rs13070844 3 12233786 intergenic variant G/A snv 0.25 2
rs75802552
IL21-AS1
4 122678167 intron variant A/- delins 0.35 2
rs2954031 8 125479491 intron variant G/T snv 0.42 8
rs11786130
PVT1
8 127992729 intron variant G/A snv 0.31 2