Disease: Neutrophil count (procedure)
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs200476039
EML6
2 54760823 intron variant TTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT delins 5.5E-02 3
rs2029582
IL1RN
2 113106194 upstream gene variant T/C snv 0.56 4
rs55799208
CXCR2
2 218135259 missense variant G/A snv 1.4E-03 1.4E-03 5
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs7575217
TBC1D8
2 101160470 intron variant A/G snv 0.68 3
rs78487399
THADA
2 43582208 intron variant G/C snv 6.2E-02 5
rs9287604 2 236867522 intergenic variant G/C snv 0.62 5
rs11359909 3 128603031 intergenic variant G/- delins 0.89 4
rs11920354
KIF9-AS1
3 47220756 intron variant C/A snv 0.34 3
rs143699489 3 141208279 intergenic variant A/G snv 0.22 4
rs6782228 3 128604581 intergenic variant G/C snv 0.28 7
rs9819371
RASA2
3 141487958 intron variant C/T snv 4.7E-02 5
rs9872570
KRBOX1 ; ACKR2
3 42855023 intron variant T/A snv 0.37 3
rs11725704 4 74094279 downstream gene variant A/G snv 0.28 5
rs11734460
PCGF3
4 711285 intron variant C/A;T snv 4
rs11931598
LOC100129931 ; TADA2B
4 7045375 intron variant C/T snv 0.55 4
rs1352846
GC
4 71752058 intron variant A/G snv 0.22 4
rs16850073
CXCL6
4 73838282 3 prime UTR variant C/T snv 0.29 5
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs28476539
SCD5
4 82631138 3 prime UTR variant G/A;T snv 3
rs58548501 4 54635119 intergenic variant -/A;ATTTTTTTTTA ins 0.43 4
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 23
rs10075801
MIR3936HG ; SLC22A4
5 132341949 intron variant A/G snv 0.31 5
rs11405616
NDFIP1
5 142130697 intron variant A/-;AA;AAA;AAAA delins 4
rs2082382 5 148820990 upstream gene variant G/A snv 0.72 5