Disease: Neutrophil count (procedure)
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs12542907 8 67900953 intergenic variant C/G snv 0.29 5
rs12550612
TNFRSF10C
8 23109256 intron variant G/A snv 0.83 5
rs12600856 17 40007042 intergenic variant T/C;G snv 5
rs12752838 1 8853597 upstream gene variant A/G snv 0.54 4
rs12936529
PIGL
17 16265470 intron variant C/T snv 0.42 3
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs1352846
GC
4 71752058 intron variant A/G snv 0.22 4
rs138488218 12 53354069 regulatory region variant A/T snv 7.6E-03 4
rs139707092
SPC25 ; NOSTRIN
2 168850753 intron variant TCTCTGGAAT/-;TCTCTGGAATTCTCTGGAAT delins 5
rs143699489 3 141208279 intergenic variant A/G snv 0.22 4
rs145013566
PNKD
2 218297998 intron variant -/C ins 5
rs146890554
CSF3
17 40017384 3 prime UTR variant C/T snv 9.6E-03 5
rs147694761
NPC1
18 23571654 intron variant AAAA/-;A;AA;AAA;AAAAA;AAAAAA delins 5
rs1570884
RCBTB1
13 49547375 intron variant A/G snv 0.58 4
rs16850073
CXCL6
4 73838282 3 prime UTR variant C/T snv 0.29 5
rs16895831 6 42548053 regulatory region variant C/T snv 0.21 3
rs16978075
LINC01478 ; LINC01601
18 44533186 intron variant T/C snv 8.5E-02 5
rs174555
FADS2 ; FADS1
11 61812288 intron variant T/C snv 0.26 3
rs17592479
COQ8A
1 226986191 intron variant T/A snv 0.41 4
rs192022
C11orf65
11 108378047 intron variant C/G;T snv 5
rs1968252
LOC105372263
19 7782850 upstream gene variant G/A;T snv 5
rs1969949
DOCK8
9 305428 intron variant T/A;C;G snv 3
rs1982094
CCDC26
8 129612570 intron variant C/T snv 4.8E-02 5
rs1991651
LOC101929248
8 10848901 downstream gene variant C/G snv 0.63 4