Disease: Neutrophil count (procedure)
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11625487
ISM2
14 77495266 intron variant G/A;C snv 0.70 2
rs2246941
LIPA
10 89245159 intron variant C/A;T snv 2
rs34891900
BCL2L13
22 17680392 intron variant C/G;T snv 2
rs546829 4 74090655 upstream gene variant A/T snv 0.63 2
rs66538782
PIK3R3 ; P3R3URF-PIK3R3
1 46130565 intron variant A/-;AA;AAA delins 2
rs8066044
MYO1C
17 1464058 upstream gene variant A/G snv 0.77 2
rs1025687
MAPK4
18 50621423 intron variant T/C snv 0.61 3
rs11920354
KIF9-AS1
3 47220756 intron variant C/A snv 0.34 3
rs12101888
EHD4
15 41939155 intron variant C/T snv 0.34 3
rs12936529
PIGL
17 16265470 intron variant C/T snv 0.42 3
rs16895831 6 42548053 regulatory region variant C/T snv 0.21 3
rs1969949
DOCK8
9 305428 intron variant T/A;C;G snv 3
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
rs28476539
SCD5
4 82631138 3 prime UTR variant G/A;T snv 3
rs305082
IRF8
16 85903372 non coding transcript exon variant T/C snv 0.28 3
rs377079849
NAA38 ; CHD3
17 7884458 intron variant ATATATATATAT/-;AT;ATAT;ATATAT;ATATATAT;ATATATATAT;ATATATATATATAT;ATATATATATATATAT;ATATATATATATATATAT;ATATATATATATATATATAT;ATATATATATATATATATATAT;ATATATATATATATATATATATAT;ATATATATATATATATATATATATAT;ATATATATATATATATATATATATATAT;ATATATATATATATATATATATATATATAT delins 0.46 3
rs4147915
ABCA7
19 1049306 synonymous variant C/A;G snv 0.18; 4.0E-06 3
rs4794822 17 40000459 downstream gene variant C/G;T snv 3
rs5820258
ARHGAP23
17 38437623 intron variant CC/-;C;CCC;CCCC;CCCCC delins 3
rs7141943
STXBP6
14 24969044 intron variant A/G;T snv 3
rs72767881
CCDC125
5 69297096 intron variant C/T snv 0.40 3
rs7405635 17 40204299 regulatory region variant T/C snv 0.34 3
rs7575217
TBC1D8
2 101160470 intron variant A/G snv 0.68 3
rs9872570
KRBOX1 ; ACKR2
3 42855023 intron variant T/A snv 0.37 3
rs10206089 2 61476184 intron variant G/A snv 4