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: rs1449263
rs1449263
1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 3 2011 2018
dbSNP: rs9880192
rs9880192
1.000 0.040 3 128578726 upstream gene variant G/A;C snv 0.31
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 3 2011 2017
dbSNP: rs3095254
rs3095254
6 31253891 intergenic variant C/A;G snv 0.55
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 2 2011 2014
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
dbSNP: rs10276619
rs10276619
1.000 0.080 7 50273756 downstream gene variant G/A snv 0.59
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2018 2018
dbSNP: rs10489481
rs10489481
1 185422035 regulatory region variant G/A snv 0.31
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs10987830
rs10987830
9 128016459 intergenic variant G/A snv 6.8E-03
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2018 2018
dbSNP: rs11086102
rs11086102
0.882 19 18287818 upstream gene variant G/C snv 0.64
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs112313229
rs112313229
3 46323369 intergenic variant G/A;T snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs112721625
rs112721625
17 59850066 upstream gene variant TT/-;T;TTT;TTTT delins
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: rs11611647
rs11611647
12 4224753 intergenic variant T/C snv 0.22
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: 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: rs11686139
rs11686139
2 226426699 intergenic variant A/C snv 0.13
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs117424492
rs117424492
15 79975053 upstream gene variant G/C;T snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2018 2018
dbSNP: rs11775706
rs11775706
8 6843366 intron variant C/G;T snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs11992162
rs11992162
8 11979005 upstream gene variant G/A;C;T snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs12149363
rs12149363
16 85895099 upstream gene variant C/G snv 7.9E-02
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2018 2018
dbSNP: rs12151289
rs12151289
19 33260946 intergenic variant G/A;C;T snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
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: 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: rs12898000
rs12898000
14 103368791 upstream gene variant G/C;T snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2018 2018
dbSNP: rs12916091
rs12916091
15 79930230 downstream gene variant T/G snv 0.53
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs12973608
rs12973608
19 18287220 upstream gene variant A/C;G snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2017 2017