Disease: Granulocyte count
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10173538
BAZ2B ; MARCHF7
2 159712765 intron variant C/G;T snv 5
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs11428934
CA11 ; SEC1P
19 48640988 intron variant -/G ins 4
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv 5
rs11734460
PCGF3
4 711285 intron variant C/A;T snv 4
rs11741826
CCDC125
5 69294573 intron variant G/A;C snv 3
rs12600856 17 40007042 intergenic variant T/C;G snv 5
rs139707092
SPC25 ; NOSTRIN
2 168850753 intron variant TCTCTGGAAT/-;TCTCTGGAATTCTCTGGAAT delins 5
rs14408
IFITM2
11 308314 missense variant T/C;G snv 0.53 4
rs145013566
PNKD
2 218297998 intron variant -/C ins 5
rs146318841
AHI1
6 135328483 intron variant TGCCATAAACCATAGCCATAG/-;TGCCATAAACCATAGCCATAGTGCCATAAACCATAGCCATAG delins 4
rs147694761
NPC1
18 23571654 intron variant AAAA/-;A;AA;AAA;AAAAA;AAAAAA delins 5
rs192022
C11orf65
11 108378047 intron variant C/G;T snv 5
rs1968252
LOC105372263
19 7782850 upstream gene variant G/A;T snv 5
rs201950044 1 161639782 intergenic variant G/T snv 5
rs2208568
LOC105373215 ; LINC02768
1 235926855 intergenic variant T/A;C;G snv 5
rs2979489
RBPMS
8 30423317 intron variant G/A;C snv 6
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs34061361
FLT3
13 28044450 intron variant AAA/-;A;AA;AAAA delins 5
rs34208856
HBS1L
6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins 6
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
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