CDK12, cyclin dependent kinase 12, 51755

N. diseases: 54; N. variants: 25
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11078902
rs11078902
17 39475630 intron variant C/G snv 0.62
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11078903
rs11078903
17 39475671 intron variant G/A;C;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11078903
rs11078903
17 39475671 intron variant G/A;C;T snv
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2012 2012
dbSNP: rs11078913
rs11078913
17 39515461 intron variant G/T snv 0.60
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11078915
rs11078915
17 39559173 intron variant T/C snv 0.62
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11650776
rs11650776
17 39485149 intron variant G/A;C snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2017 2017
dbSNP: rs11657153
rs11657153
17 39543476 intron variant A/G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11658678
rs11658678
17 39523843 intron variant C/A;G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs12449852
rs12449852
1.000 0.080 17 39475835 intron variant A/G snv 0.79
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs12449852
rs12449852
1.000 0.080 17 39475835 intron variant A/G snv 0.79
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs12449852
rs12449852
1.000 0.080 17 39475835 intron variant A/G snv 0.79
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs12451586
rs12451586
17 39477582 intron variant T/A snv 0.61
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2017 2017
dbSNP: rs12451586
rs12451586
17 39477582 intron variant T/A snv 0.61
Creatinine measurement, serum (procedure)
0.700 1.000 1 2017 2017
dbSNP: rs12936996
rs12936996
17 39509301 intron variant G/A;C snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs2303316
rs2303316
17 39547964 intron variant A/G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4239222
rs4239222
17 39539982 intron variant G/T snv 0.67
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4488484
rs4488484
17 39561124 intron variant T/A snv 0.79
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4794813
rs4794813
17 39514741 intron variant A/G;T snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2019 2019
dbSNP: rs4794814
rs4794814
17 39540599 intron variant G/A snv 0.62
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2019 2019
dbSNP: rs4795384
rs4795384
17 39560518 intron variant C/G snv 0.68
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2019 2019
dbSNP: rs4795384
rs4795384
17 39560518 intron variant C/G snv 0.68
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs6503521
rs6503521
17 39559298 intron variant G/A;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs7216086
rs7216086
17 39553169 intron variant G/A snv 0.60
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs72825193
rs72825193
17 39459491 upstream gene variant T/C snv 1.3E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs7503069
rs7503069
17 39540875 intron variant C/G snv 0.62
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012