CDK6, cyclin dependent kinase 6, 1021

N. diseases: 266; N. variants: 27
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: rs445
rs445 		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 		7 92779056 intron variant C/T snv 0.14
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.800 1.000 4 2011 2019
dbSNP: rs4272
rs4272 		1.000 0.120 7 92607515 3 prime UTR variant A/G;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.800 1.000 2 2014 2019
dbSNP: rs606231255
rs606231255 		1.000 7 92671484 missense variant C/T snv 7.0E-06
CUI: C4015156
Disease: MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE
MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE 		0.800 0
dbSNP: rs2282978
rs2282978 		7 92635096 intron variant T/C snv 0.38
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2008 2009
dbSNP: rs2282978
rs2282978 		7 92635096 intron variant T/C snv 0.38
CUI: C0489786
Disease: Height
Height 		0.700 1.000 3 2008 2009
dbSNP: rs445
rs445 		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: rs2040494
rs2040494 		7 92627591 intron variant C/T snv 0.64
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2008 2009
dbSNP: rs42039
rs42039 		1.000 0.080 7 92615108 3 prime UTR variant C/T snv 0.19 0.19
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2014 2019
dbSNP: rs42235
rs42235 		7 92618762 intron variant C/T snv 0.32
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2010 2013
dbSNP: rs42235
rs42235 		7 92618762 intron variant C/T snv 0.32
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs42377
rs42377 		7 92614358 3 prime UTR variant G/A snv 0.28
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2017 2019
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: rs445
rs445 		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: rs8179
rs8179 		0.882 0.080 7 92606850 3 prime UTR variant T/A;C;G snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs8179
rs8179 		0.882 0.080 7 92606850 3 prime UTR variant T/A;C;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs10225965
rs10225965 		7 92644264 intron variant C/T snv 0.26
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs10269774
rs10269774 		7 92624658 intron variant G/A snv 0.36
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs10269774
rs10269774 		7 92624658 intron variant G/A snv 0.36
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs11773884
rs11773884 		1.000 0.080 7 92655809 intron variant A/G snv 0.36
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs2040494
rs2040494 		7 92627591 intron variant C/T snv 0.64
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2008 2008
dbSNP: rs2040494
rs2040494 		7 92627591 intron variant C/T snv 0.64
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2018 2018
dbSNP: rs2282978
rs2282978 		7 92635096 intron variant T/C snv 0.38
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2019 2019
dbSNP: rs2282978
rs2282978 		7 92635096 intron variant T/C snv 0.38
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs2282978
rs2282978 		7 92635096 intron variant T/C snv 0.38
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019