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: rs2227532
rs2227532
0.882 0.120 4 73739815 upstream gene variant T/C snv 2.9E-02
CUI: C0031099
Disease: Periodontitis
Periodontitis
0.020 0.500 2 2015 2017
dbSNP: rs2227532
rs2227532
0.882 0.120 4 73739815 upstream gene variant T/C snv 2.9E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs2227532
rs2227532
0.882 0.120 4 73739815 upstream gene variant T/C snv 2.9E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2015 2015
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.050 0.800 5 2010 2019
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.050 0.800 5 2010 2019
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.040 1.000 4 2012 2018
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.040 1.000 4 2012 2018
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.040 1.000 4 2015 2019
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.040 0.750 4 2014 2020
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.020 1.000 2 2019 2019
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
0.020 1.000 2 2013 2019
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0031099
Disease: Periodontitis
Periodontitis
0.020 0.500 2 2015 2017
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
Exudative age-related macular degeneration
0.020 1.000 2 2015 2016
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.020 1.000 2 2014 2018
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.020 1.000 2 2019 2019
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
Liver and Intrahepatic Biliary Tract Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0036690
Disease: Septicemia
Septicemia
0.010 1.000 1 2016 2016
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II
0.010 < 0.001 1 2015 2015
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0031106
Disease: Aggressive Periodontitis
Aggressive Periodontitis
0.010 < 0.001 1 2013 2013
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee
0.010 < 0.001 1 2019 2019
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.010 1.000 1 2016 2016
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0024115
Disease: Lung diseases
Lung diseases
0.010 1.000 1 2016 2016
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0030809
Disease: Pemphigus Vulgaris
Pemphigus Vulgaris
0.010 1.000 1 2019 2019