Disease: Eosinophil count procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10165200
LINC00299
2 8299499 intron variant G/A snv 0.36 2
rs10265538 7 20502242 intergenic variant T/C snv 0.20 2
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
rs1036332
LINC01221
1 199043349 intron variant A/C snv 0.70 2
rs10410864 19 39711776 downstream gene variant T/C snv 0.68 2
rs10542411 2 61541105 upstream gene variant ATATT/-;ATATTATATT delins 0.23 2
rs10852622
ZFPM1
16 88490472 intron variant A/G snv 0.35 2
rs10893844 11 128315955 regulatory region variant G/C snv 0.36 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
rs111759324 1 101186966 upstream gene variant C/T snv 0.11 2
rs11319879
HHEX
10 92693719 intron variant A/- delins 0.53 2
rs113422568
SUFU
10 102578181 intron variant G/A snv 0.25 2
rs11353326
ARIH2
3 48941172 intron variant AAAAA/-;A;AA;AAA;AAAA;AAAAAA;AAAAAAA delins 2
rs113604586
ALOX15
17 4639054 missense variant T/C snv 1.7E-03 1.6E-03 2
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
rs11555542
ASB2
14 93951185 missense variant T/C snv 3.3E-02 3.7E-02 2
rs11669910
EXOC3L2 ; MARK4
19 45238075 intron variant A/T snv 0.23 2
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
rs12264390
LARP4B
10 913171 intron variant T/C snv 0.20 2
rs12408934
JAK1
1 64957764 intron variant G/A snv 6.1E-02 2
rs12413946
ZNF365
10 62671446 non coding transcript exon variant T/C snv 6.2E-02 2