Disease: Neutrophil count (procedure)
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34208856
HBS1L
6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins 6
rs34293785 1 65671509 intergenic variant T/C snv 4
rs34891900
BCL2L13
22 17680392 intron variant C/G;T snv 2
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs3917914
CSF3R
1 36482287 intron variant G/A;T snv 5
rs397731840
CCDC26
8 129599504 intron variant TT/-;T;TTT;TTTT;TTTTT delins 5
rs397933924 10 97314229 upstream gene variant -/CAGGTTCAAGCGA ins 5
rs398032702
C18orf25
18 46245574 intron variant AA/-;A;AAA;AAAA;AAAAAAA;AAAAAAAAAAAAA delins 4
rs4147915
ABCA7
19 1049306 synonymous variant C/A;G snv 0.18; 4.0E-06 3
rs575404063 19 18405498 intergenic variant AAA/-;A;AA;AAAA;AAAAA delins 4
rs5820258
ARHGAP23
17 38437623 intron variant CC/-;C;CCC;CCCC;CCCCC delins 3
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs6500550
TRAP1
16 3696240 intron variant C/G;T snv 5
rs66538782
PIK3R3 ; P3R3URF-PIK3R3
1 46130565 intron variant A/-;AA;AAA delins 2
rs71191701 9 136427805 downstream gene variant G/C;T snv 4
rs7141943
STXBP6
14 24969044 intron variant A/G;T snv 3
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs778387 1 56158423 intron variant C/A;G;T snv 4
rs791357
LOC107986482
5 173778222 downstream gene variant T/A;C snv 4
rs8179
CDK6
0.882 0.080 7 92606850 3 prime UTR variant T/A;C;G snv 5
rs8705
ETS1
11 128459018 3 prime UTR variant G/A;T snv 5
rs555346412
HECTD4
12 112191863 intron variant G/C snv 8.2E-04 5
rs55799208
CXCR2
2 218135259 missense variant G/A snv 1.4E-03 1.4E-03 5
rs143034248
JAML
11 118210555 missense variant C/T snv 4.0E-03 3.5E-03 7