CD33, CD33 molecule, 945

N. diseases: 142; N. variants: 6
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: rs3865444
rs3865444
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.900 1.000 16 2011 2019
dbSNP: rs12459419
rs12459419
0.925 0.120 19 51225221 missense variant C/G;T snv 0.31
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs12459419
rs12459419
0.925 0.120 19 51225221 missense variant C/G;T snv 0.31
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs12459419
rs12459419
0.925 0.120 19 51225221 missense variant C/G;T snv 0.31
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs12459419
rs12459419
0.925 0.120 19 51225221 missense variant C/G;T snv 0.31
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs1354106
rs1354106
19 51234736 intron variant T/G snv 0.38
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs201074739
rs201074739
19 51225848 frameshift variant GGCC/- delins 1.4E-02 1.6E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs2455069
rs2455069
19 51225385 missense variant A/G snv 0.35 0.42
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2019 2019
dbSNP: rs3865444
rs3865444
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25
CUI: C0162534
Disease: Prion Diseases
Prion Diseases
Infections; Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs3865444
rs3865444
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs3865444
rs3865444
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2016 2016
dbSNP: rs3865444
rs3865444
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs3865444
rs3865444
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
Nervous System Diseases; Mental Disorders 0.040 1.000 4 2015 2019
dbSNP: rs3826656
rs3826656
0.925 0.080 19 51223357 upstream gene variant G/A snv 0.76
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.020 0.500 2 2018 2019
dbSNP: rs12459419
rs12459419
0.925 0.120 19 51225221 missense variant C/G;T snv 0.31
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs12459419
rs12459419
0.925 0.120 19 51225221 missense variant C/G;T snv 0.31
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs3826656
rs3826656
0.925 0.080 19 51223357 upstream gene variant G/A snv 0.76
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs3865444
rs3865444
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs3865444
rs3865444
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014