KAT2B, lysine acetyltransferase 2B, 8850

N. diseases: 116; N. variants: 9
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: rs12636078
rs12636078 		3 20064181 intron variant A/G;T snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 2 2016 2019
dbSNP: rs12636078
rs12636078 		3 20064181 intron variant A/G;T snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs12636078
rs12636078 		3 20064181 intron variant A/G;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2623079
rs2623079 		3 20069953 intron variant C/A;G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs2948094
rs2948094 		3 20070116 intron variant G/A;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2948097
rs2948097 		3 20063934 intron variant A/G snv 0.65
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2018 2018
dbSNP: rs4858757
rs4858757 		3 20075547 intron variant T/G snv 0.44
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs4858758
rs4858758 		3 20075741 intron variant C/T snv 0.41
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs9829896
rs9829896 		3 20135980 intron variant C/A;T snv
CUI: C0236969
Disease: Substance-Related Disorders
Substance-Related Disorders 		Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2016 2016
dbSNP: rs9874923
rs9874923 		3 20060071 intron variant C/G;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2013 2013
dbSNP: rs9874923
rs9874923 		3 20060071 intron variant C/G;T snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2013 2013
dbSNP: rs17006625
rs17006625 		0.925 0.080 3 20119604 missense variant A/C;G snv 4.0E-06; 3.3E-02
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2012 2016
dbSNP: rs17006625
rs17006625 		0.925 0.080 3 20119604 missense variant A/C;G snv 4.0E-06; 3.3E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 < 0.001 1 2000 2000
dbSNP: rs17006625
rs17006625 		0.925 0.080 3 20119604 missense variant A/C;G snv 4.0E-06; 3.3E-02
CUI: C0017638
Disease: Glioma
Glioma 		Neoplasms 0.010 < 0.001 1 2000 2000
dbSNP: rs9829896
rs9829896 		3 20135980 intron variant C/A;T snv
CUI: C0013146
Disease: Drug abuse
Drug abuse 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2016 2016