rs445, CDK6

N. diseases: 9
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 7 92779056 intron variant C/T snv 0.14 0.800 1.000 7 2010 2019
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 7 92779056 intron variant C/T snv 0.14 0.800 1.000 4 2011 2019
Neutrophil count (procedure)
CUI: C0200633
Disease: Neutrophil count (procedure)
234 7 92779056 intron variant C/T snv 0.14 0.700 1.000 3 2011 2018
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
296 7 92779056 intron variant C/T snv 0.14 0.700 1.000 2 2016 2018
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
296 7 92779056 intron variant C/T snv 0.14 0.700 1.000 2 2016 2018
Blood basophil count (lab test)
CUI: C0200641
Disease: Blood basophil count (lab test)
452 7 92779056 intron variant C/T snv 0.14 0.700 1.000 1 2016 2016
Body Height
CUI: C0005890
Disease: Body Height
3972 7 92779056 intron variant C/T snv 0.14 0.700 1.000 1 2019 2019
Granulocyte count
CUI: C0857490
Disease: Granulocyte count
150 7 92779056 intron variant C/T snv 0.14 0.700 1.000 1 2016 2016
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 7 92779056 intron variant C/T snv 0.14 0.700 1.000 1 2018 2018