Disease: Neutrophil count (procedure)
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10075801
MIR3936HG ; SLC22A4
5 132341949 intron variant A/G snv 0.31 5
rs10138752
RAD51B
14 68713254 intron variant C/T snv 8.8E-02 5
rs10173538
BAZ2B ; MARCHF7
2 159712765 intron variant C/G;T snv 5
rs1025688
MAPK4
18 50621506 intron variant G/A snv 0.35 3
rs111930700
ACVR1B
12 51967869 intron variant C/G snv 8.4E-02 4
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs11361923
NOXRED1
14 77396337 intron variant C/- delins 0.54 4
rs11428934
CA11 ; SEC1P
19 48640988 intron variant -/G ins 4
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv 5
rs11654074
VMP1
17 59748211 intron variant A/C snv 0.40 5
rs11734460
PCGF3
4 711285 intron variant C/A;T snv 4
rs11741826
CCDC125
5 69294573 intron variant G/A;C snv 3
rs11769630 7 50218107 intron variant T/A snv 5.4E-02 4
rs11931598
LOC100129931 ; TADA2B
4 7045375 intron variant C/T snv 0.55 4
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 7
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26 7
rs12550612
TNFRSF10C
8 23109256 intron variant G/A snv 0.83 5
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs1334577
RREB1
0.925 0.120 6 7211518 intron variant G/A snv 0.23 2
rs1352846
GC
4 71752058 intron variant A/G snv 0.22 4
rs139707092
SPC25 ; NOSTRIN
2 168850753 intron variant TCTCTGGAAT/-;TCTCTGGAATTCTCTGGAAT delins 5
rs140578741
BRD3
9 134042697 intron variant CATATATATACACA/- delins 0.24 2
rs145013566
PNKD
2 218297998 intron variant -/C ins 5
rs146091102
PIGV
1 26795439 intron variant G/A snv 2.2E-02 2
rs146318841
AHI1
6 135328483 intron variant TGCCATAAACCATAGCCATAG/-;TGCCATAAACCATAGCCATAGTGCCATAAACCATAGCCATAG delins 4