Disease: Neutrophil count (procedure)
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11137087 8 7048518 intergenic variant A/G snv 0.60 2
rs12593998
SPPL2A
15 50766432 upstream gene variant A/C;G snv 2
rs1334577
RREB1
0.925 0.120 6 7211518 intron variant G/A snv 0.23 2
rs140578741
BRD3
9 134042697 intron variant CATATATATACACA/- delins 0.24 2
rs146091102
PIGV
1 26795439 intron variant G/A snv 2.2E-02 2
rs150616068
PCDHA5 ; PCDHA7 ; PCDHA9 ; PCDHA1 ; PCDHA2 ; PCDHA6 ; PCDHA4 ; PCDHA12 ; PCDHA3 ; PCDHA10 ; PCDHA11 ; PCDHA8 ; PCDHA13
5 140904631 intron variant G/A snv 2.9E-02 2
rs1567558
PXYLP1
3 141289281 intron variant A/G snv 0.50 2
rs1999537 1 56439852 intron variant G/A snv 0.89 2
rs201399927 2 24377011 intergenic variant TT/-;T;TTT;TTTT delins 0.18 2
rs2251188 7 6664701 intron variant A/G snv 0.71 2
rs2451279
LOC112267968
6 159094045 intron variant A/G snv 0.73 2
rs34115320
ZNF786
7 149086845 intron variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT delins 0.57 2
rs35955747
DRG1
22 31417072 intron variant A/G;T snv 2
rs3742716
RIN3
14 92652324 synonymous variant G/A snv 0.32 0.25 2
rs61897795
FADS2
11 61850697 intron variant A/G snv 9.5E-02 2
rs6928836 6 22880684 intron variant G/C;T snv 0.16 2
rs72917514
EML6
2 54786509 intron variant G/A snv 0.11 2
rs9926664
IRF8
16 85905149 intron variant A/G snv 0.19 2
rs1025688
MAPK4
18 50621506 intron variant G/A snv 0.35 3
rs11741826
CCDC125
5 69294573 intron variant G/A;C snv 3
rs13187922 5 142083096 intergenic variant C/T snv 0.48 3
rs16895831 6 42548053 regulatory region variant C/T snv 0.21 3
rs3209441
DOCK8
9 286491 missense variant G/A snv 0.12 0.11 3
rs4147915
ABCA7
19 1049306 synonymous variant C/A;G snv 0.18; 4.0E-06 3
rs4924590
EHD4
15 41941475 intron variant T/A snv 0.30 3