Source: BEFREE

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: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
Diabetes Mellitus, Non-Insulin-Dependent
0.050 1.000 5 2010 2019
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.050 0.800 5 2010 2020
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.040 0.750 4 2015 2020
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0004096
Disease: Asthma
Asthma
0.040 1.000 4 2014 2019
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.040 0.750 4 2009 2014
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
0.040 1.000 4 2017 2019
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.040 1.000 4 2013 2018
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.030 1.000 3 2014 2016
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0006271
Disease: Bronchiolitis
Bronchiolitis
0.030 1.000 3 2017 2019
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.030 1.000 3 2012 2016
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.030 0.667 3 2018 2019
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.030 0.333 3 2012 2014
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.030 0.667 3 2011 2017
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.030 1.000 3 2007 2016
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
0.030 0.667 3 2013 2017
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.030 0.667 3 2011 2017
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.030 1.000 3 2013 2017
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.030 0.333 3 2012 2014
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0243026
Disease: Sepsis
Sepsis
0.020 1.000 2 2010 2016
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
0.020 1.000 2 2015 2016
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.020 < 0.001 2 2017 2019
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.020 1.000 2 2012 2019
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0343641
Disease: Human papilloma virus infection
Human papilloma virus infection
0.020 1.000 2 2015 2019
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.020 1.000 2 2015 2016
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
0.020 1.000 2 2015 2016