Source: GWASCAT

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: rs445
rs445
CDK6
7 92779056 intron variant C/T snv 0.14
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.800 1.000 7 2010 2019
dbSNP: rs445
rs445
CDK6
7 92779056 intron variant C/T snv 0.14
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.800 1.000 3 2011 2019
dbSNP: rs445
rs445
CDK6
7 92779056 intron variant C/T snv 0.14
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 3 2011 2018
dbSNP: rs445
rs445
CDK6
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: rs445
rs445
CDK6
7 92779056 intron variant C/T snv 0.14
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 2 2016 2018
dbSNP: rs445
rs445
CDK6
7 92779056 intron variant C/T snv 0.14
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs445
rs445
CDK6
7 92779056 intron variant C/T snv 0.14
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs445
rs445
CDK6
7 92779056 intron variant C/T snv 0.14
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs445
rs445
CDK6
7 92779056 intron variant C/T snv 0.14
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016