rs1803274, BCHE

N. diseases: 13
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.
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 0.800 1.000 2 2011 2011
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 0.700 1.000 1 2018 2018
Butyrylcholinesterase deficiency
CUI: C1283400
Disease: Butyrylcholinesterase deficiency
43 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 0.700 0
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 0.040 1.000 4 2004 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 0.020 1.000 2 2008 2010
Addictive Behavior
CUI: C0085281
Disease: Addictive Behavior
56 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 0.010 1.000 1 2019 2019
cocaine use
CUI: C3496069
Disease: cocaine use
8 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 0.010 1.000 1 2013 2013
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 0.010 1.000 1 2008 2008
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 0.010 1.000 1 2008 2008
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 0.010 1.000 1 2004 2004
Obesity
CUI: C0028754
Disease: Obesity
1111 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 0.010 1.000 1 2019 2019
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 0.010 1.000 1 2018 2018
Substance abuse problem
CUI: C0740858
Disease: Substance abuse problem
20 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 0.010 1.000 1 2019 2019