Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11190141
rs11190141
1.000 0.040 10 99532633 upstream gene variant C/T snv 0.40
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs6584283
rs6584283
0.776 0.080 10 99530544 intron variant T/C snv 0.56
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2018 2018
dbSNP: rs11189181
rs11189181
10 97384397 intron variant A/G snv 0.30
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs4919087
rs4919087
10 97312750 upstream gene variant A/G;T snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs7516138
rs7516138
1 9651584 upstream gene variant A/G snv 0.52
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs75963851
rs75963851
11 95363157 intergenic variant A/G snv 3.1E-03
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2018 2018
dbSNP: rs445
rs445
7 92779056 intron variant C/T snv 0.14
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 2 2016 2018
dbSNP: rs72699818
rs72699818
14 92611266 intron variant T/C snv 0.12
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs12753280
rs12753280
1 92550671 intron variant T/A;C snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs115340020
rs115340020
1 92300881 intron variant G/A snv 1.7E-02
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs141094656
rs141094656
1 92287779 intron variant T/C snv 1.3E-02
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs35761782
rs35761782
12 89504600 intron variant -/T delins 0.70
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs62551476
rs62551476
9 88978375 downstream gene variant T/C snv 0.15
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs1157008
rs1157008
9 88920798 regulatory region variant T/C;G snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs9410380
rs9410380
9 88838716 regulatory region variant T/C snv 0.47
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs4432538
rs4432538
20 8626746 intron variant G/A snv 0.52
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs11642657
rs11642657
16 85982722 intron variant C/A;T snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs9674233
rs9674233
16 85978993 intron variant T/C;G snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2018 2018
dbSNP: rs12232384
rs12232384
16 85976154 intron variant C/A;T snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs142105922
rs142105922
16 85968988 intron variant TAATAA/-;TAA;TAATAATAA;TAATAATAATAA;TAATAATAATAATAA delins
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs11640143
rs11640143
16 85955858 regulatory region variant T/C;G snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs6540234
rs6540234
16 85949450 downstream gene variant T/C snv 0.78
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs4843869
rs4843869
16 85941535 intron variant G/A snv 0.18
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2018 2018
dbSNP: rs12711490
rs12711490
0.925 0.080 16 85939422 intron variant T/C snv 0.18
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs1021479
rs1021479
16 85923808 upstream gene variant T/A;C snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2018 2018