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: rs35349669
rs35349669 		0.925 0.080 2 233159830 intron variant C/T snv 0.35
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.800 1.000 3 2013 2019
dbSNP: rs1057258
rs1057258 		2 233206983 3 prime UTR variant C/T snv 0.30
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs10933431
rs10933431 		1.000 0.080 2 233117202 intron variant G/C snv 0.63
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 2 2018 2019
dbSNP: rs1057258
rs1057258 		2 233206983 3 prime UTR variant C/T snv 0.30
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs1057258
rs1057258 		2 233206983 3 prime UTR variant C/T snv 0.30
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs4246649
rs4246649 		2 233060781 intron variant A/G snv 0.90
CUI: C0009928
Disease: Contrast Sensitivity
Contrast Sensitivity 		0.700 1.000 1 2014 2014
dbSNP: rs56235204
rs56235204 		2 233205887 intron variant T/- del 0.19
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs6708049
rs6708049 		2 233078583 intron variant T/A;C snv 0.82
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs76999017
rs76999017 		1.000 0.040 2 233067548 intron variant G/C snv 1.4E-02
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.700 1.000 1 2016 2016
dbSNP: rs9247
rs9247 		0.925 0.080 2 233204655 missense variant C/A;T snv 1.0E-05; 0.22
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1205046029
rs1205046029 		1.000 0.040 2 233164391 missense variant G/A snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs12987960
rs12987960 		1.000 0.040 2 233199308 intron variant A/G snv
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
Pseudohyperkalemia Cardiff 		Nutritional and Metabolic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs35349669
rs35349669 		0.925 0.080 2 233159830 intron variant C/T snv 0.35
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset 		Nervous System Diseases; Mental Disorders 0.010 < 0.001 1 2016 2016
dbSNP: rs61068452
rs61068452 		1.000 0.080 2 233105789 intron variant A/G snv 0.17
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs763156019
rs763156019 		1.000 0.040 2 233204611 missense variant A/T snv 2.3E-05 7.0E-06
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs9247
rs9247 		0.925 0.080 2 233204655 missense variant C/A;T snv 1.0E-05; 0.22
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.010 1.000 1 2012 2012