Disease: Monocyte count procedure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs413141 19 6675978 downstream gene variant A/G snv 0.84 4
rs61745454
CCDC69
5 151187456 missense variant A/G snv 3.7E-02 4.6E-02 5
rs75963851 11 95363157 intergenic variant A/G snv 3.1E-03 3
rs1800973
LYZ
0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 9
rs1700159
ACVRL1
1.000 0.040 12 51912002 intron variant C/A;G;T snv 4
rs11642657 16 85982722 intron variant C/A;T snv 3
rs13138355 4 82624823 upstream gene variant C/A;T snv 4
rs2238783
ARVCF
22 19984929 intron variant C/G snv 0.42 3
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26 7
rs143034248
JAML
11 118210555 missense variant C/T snv 4.0E-03 3.5E-03 7
rs1449263 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 5
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs34599082
ACKR1 ; CADM3-AS1
1 159205704 missense variant C/T snv 1.1E-02 9.9E-03 8
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs7296503
PDZRN4
12 41306962 intron variant C/T snv 0.57 13
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03 13
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs1375493
ITGA4
2 181459039 non coding transcript exon variant G/A snv 0.56 3
rs2615061
LOC102723834
1 225708104 intron variant G/A snv 0.12 3
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48