Disease: Monocyte count result
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 24
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
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
rs9917425
OTOR
20 16755400 intron variant G/T snv 0.16 13
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs2228467
CYP8B1 ; KRBOX1 ; ACKR2
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02 8
rs34599082
ACKR1 ; CADM3-AS1
1 159205704 missense variant C/T snv 1.1E-02 9.9E-03 8
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
rs2038700
STXBP6
14 24992783 intron variant T/C snv 0.53 7
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 7
rs6782228 3 128604581 intergenic variant G/C snv 0.28 7
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24 7
rs2239630
CEBPE
0.925 0.160 14 23120140 upstream gene variant A/C;G snv 6
rs1449263 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 5