Disease: Eosinophil count procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11428934
CA11 ; SEC1P
19 48640988 intron variant -/G ins 4
rs145013566
PNKD
2 218297998 intron variant -/C ins 5
rs397933924 10 97314229 upstream gene variant -/CAGGTTCAAGCGA ins 5
rs58548501 4 54635119 intergenic variant -/A;ATTTTTTTTTA ins 0.43 4
rs10542411 2 61541105 upstream gene variant ATATT/-;ATATTATATT delins 0.23 2
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs11319879
HHEX
10 92693719 intron variant A/- delins 0.53 2
rs11327184
CCDC26
8 129592027 intron variant C/- delins 0.40 4
rs11353326
ARIH2
3 48941172 intron variant AAAAA/-;A;AA;AAA;AAAA;AAAAAA;AAAAAAA delins 2
rs11359909 3 128603031 intergenic variant G/- delins 0.89 4
rs139707092
SPC25 ; NOSTRIN
2 168850753 intron variant TCTCTGGAAT/-;TCTCTGGAATTCTCTGGAAT delins 5
rs140948517
RHBDD2
7 75857462 intron variant TT/-;T;TTT;TTTT;TTTTTTTTTTTT delins 2
rs147694761
NPC1
18 23571654 intron variant AAAA/-;A;AA;AAA;AAAAA;AAAAAA delins 5
rs200638392 6 87128241 intergenic variant GAT/-;GATGAT delins 0.47 5
rs34020101
IL18RAP
2 102435015 non coding transcript exon variant AA/-;A;AAA delins 2
rs34061361
FLT3
13 28044450 intron variant AAA/-;A;AA;AAAA delins 5
rs34149660 9 133001720 intergenic variant AAAAAAAAAAAAA/-;AAAAAA;AAAAAAA;AAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAA;AAAAAAAAAAAAAA;AAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAA delins 0.31 2
rs34208856
HBS1L
6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins 6
rs34332679 14 35412760 regulatory region variant -/A;AA delins 2
rs34675278 5 98808491 intergenic variant AA/-;A;AAA;AAAA;AAAAA delins 2
rs34686164
MAP3K11
11 65601756 intron variant AAAAA/-;AA;AAA;AAAA;AAAAAA;AAAAAAA;AAAAAAAAAAAA delins 0.43 2
rs34762051 17 40007650 downstream gene variant AA/-;A;AAA delins 0.31 5
rs36058533 2 96570916 intergenic variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTT delins 2
rs36229146 7 22744868 downstream gene variant AATATATATATATATATATATATATA/- delins 7.2E-02 2
rs3831732
PTEN
10 87895485 intron variant -/A;AA delins 2