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: rs16969968
rs16969968
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.030 1.000 3 2011 2019
dbSNP: rs8192482
rs8192482
1.000 0.040 15 78593856 3 prime UTR variant C/T snv 0.24
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
Respiratory Tract Diseases 0.700 1.000 2 2015 2019
dbSNP: rs16969968
rs16969968
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24
CUI: C0009241
Disease: Cognition Disorders
Cognition Disorders
Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs16969968
rs16969968
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24
CUI: C0871189
Disease: Psychotic symptom
Psychotic symptom
0.010 1.000 1 2019 2019
dbSNP: rs16969968
rs16969968
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24
CUI: C3887461
Disease: Head and Neck Carcinoma
Head and Neck Carcinoma
Neoplasms 0.010 < 0.001 1 2019 2019
dbSNP: rs16969968
rs16969968
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs16969968
rs16969968
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
Malignant Head and Neck Neoplasm
Neoplasms 0.010 < 0.001 1 2019 2019
dbSNP: rs17486278
rs17486278
0.827 0.120 15 78575140 intron variant A/C snv 0.32
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs55781567
rs55781567
0.851 0.080 15 78565644 5 prime UTR variant C/G snv 0.31
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2019 2019
dbSNP: rs55781567
rs55781567
0.851 0.080 15 78565644 5 prime UTR variant C/G snv 0.31
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
Neoplasms; Respiratory Tract Diseases 0.700 1.000 1 2019 2019
dbSNP: rs16969968
rs16969968
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24
CUI: C0028043
Disease: Nicotine Dependence
Nicotine Dependence
Chemically-Induced Disorders; Mental Disorders 0.100 1.000 29 2008 2018
dbSNP: rs16969968
rs16969968
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.100 0.963 27 2008 2018
dbSNP: rs16969968
rs16969968
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.100 0.963 27 2008 2018
dbSNP: rs16969968
rs16969968
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.100 0.963 27 2008 2018
dbSNP: rs16969968
rs16969968
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
Respiratory Tract Diseases 0.780 0.889 9 2010 2018
dbSNP: rs16969968
rs16969968
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs16969968
rs16969968
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs16969968
rs16969968
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs16969968
rs16969968
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.030 0.667 3 2010 2017
dbSNP: rs16969968
rs16969968
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.030 0.667 3 2010 2017
dbSNP: rs17486278
rs17486278
0.827 0.120 15 78575140 intron variant A/C snv 0.32
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
Respiratory Tract Diseases 0.700 1.000 3 2015 2017
dbSNP: rs55781567
rs55781567
0.851 0.080 15 78565644 5 prime UTR variant C/G snv 0.31
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.700 1.000 2 2016 2017
dbSNP: rs55781567
rs55781567
0.851 0.080 15 78565644 5 prime UTR variant C/G snv 0.31
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
Neoplasms 0.710 1.000 2 2013 2017
dbSNP: rs149941240
rs149941240
1.000 0.080 15 78591694 intron variant CCTT/- delins 6.3E-03
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs16969968
rs16969968
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2017 2017