Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease
0.010 1.000 1 2018 2018
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C1096063
Disease: Drug Resistant Epilepsy
Drug Resistant Epilepsy
0.010 1.000 1 2016 2016
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity
0.010 1.000 1 2016 2016
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.010 1.000 1 2016 2016
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.010 1.000 1 2012 2012
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0748355
Disease: Acute respiratory distress
Acute respiratory distress
0.010 1.000 1 2019 2019
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction
0.010 1.000 1 2017 2017
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C2363774
Disease: Neutrophilic asthma
Neutrophilic asthma
0.010 1.000 1 2018 2018
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.010 1.000 1 2013 2013
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.010 1.000 1 2019 2019
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0497327
Disease: Dementia
Dementia
0.010 1.000 1 2019 2019
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.010 1.000 1 2014 2014
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C4744444
Disease: Metastatic Lung Adenocarcinoma
Metastatic Lung Adenocarcinoma
0.010 1.000 1 2017 2017
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.010 1.000 1 2016 2016
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
0.010 1.000 1 2015 2015
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.010 1.000 1 2005 2005
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0947751
Disease: Vascular inflammations
Vascular inflammations
0.010 1.000 1 2010 2010
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.010 1.000 1 2019 2019
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.010 1.000 1 2005 2005
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.010 1.000 1 2010 2010
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0011875
Disease: Diabetic Angiopathies
Diabetic Angiopathies
0.010 1.000 1 2014 2014
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung
0.010 1.000 1 2018 2018
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0020179
Disease: Huntington Disease
Huntington Disease
0.010 1.000 1 2010 2010
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C0003864
Disease: Arthritis
Arthritis
0.010 1.000 1 2002 2002