Disease: Neutrophil count (procedure)
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7168592
CHSY1
15 101183294 intron variant C/T snv 9.8E-02 4
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs2436845
AZIN1
8 102840179 intron variant G/A snv 0.37 4
rs4147915
ABCA7
19 1049306 synonymous variant C/A;G snv 0.18; 4.0E-06 3
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 23
rs663045
SLC25A24
1 108200437 5 prime UTR variant G/C snv 0.55 5
rs192022
C11orf65
11 108378047 intron variant C/G;T snv 5
rs1991651
LOC101929248
8 10848901 downstream gene variant C/G snv 0.63 4
rs9400271
CCDC162P
6 109286353 non coding transcript exon variant G/A snv 0.51 5
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs555346412
HECTD4
12 112191863 intron variant G/C snv 8.2E-04 5
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
rs143034248
JAML
11 118210555 missense variant C/T snv 4.0E-03 3.5E-03 7
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
rs2954031 8 125479491 intron variant G/T snv 0.42 8
rs8705
ETS1
11 128459018 3 prime UTR variant G/A;T snv 5
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs11359909 3 128603031 intergenic variant G/- delins 0.89 4
rs6782228 3 128604581 intergenic variant G/C snv 0.28 7
rs397731840
CCDC26
8 129599504 intron variant TT/-;T;TTT;TTTT;TTTTT delins 5
rs1982094
CCDC26
8 129612570 intron variant C/T snv 4.8E-02 5