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: rs1518111
rs1518111
0.790 0.360 1 206771300 intron variant T/C snv 0.71
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.830 1.000 3 2010 2015
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.830 0.800 3 2010 2017
dbSNP: rs3024493
rs3024493
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.720 1.000 2 2013 2019
dbSNP: rs3024490
rs3024490
0.742 0.520 1 206771966 intron variant A/C;G;T snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.710 0.500 1 2013 2017
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: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.040 1.000 4 2011 2019
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.040 0.750 4 2012 2018
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.040 0.750 4 2012 2018
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.040 1.000 4 2011 2019
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.040 1.000 4 2012 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: 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: C0019196
Disease: Hepatitis C
Hepatitis C
0.040 1.000 4 2013 2018
dbSNP: rs145922845
rs145922845
1.000 0.040 1 206772393 missense variant C/T snv 1.9E-03 1.8E-03
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.030 0.667 3 2000 2005
dbSNP: rs1554286
rs1554286
0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.030 1.000 3 2012 2015
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.030 0.667 3 2013 2016
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.030 0.333 3 2012 2018
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
Diabetes Mellitus, Non-Insulin-Dependent
0.030 1.000 3 2010 2014
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
0.030 1.000 3 2008 2016
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary
0.030 1.000 3 2011 2018
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.030 1.000 3 2013 2018
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.030 0.667 3 2014 2017