rs3184504, SH2B3;ATXN2

N. diseases: 29
Source: BEFREE ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
769 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.820 1.000 2 2011 2018
Diabetes Mellitus, Insulin-Dependent
388 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.820 1.000 2 2009 2018
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
76 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.810 1.000 1 2011 2015
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1022 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.810 1.000 1 2013 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1186 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.730 1.000 3 2015 2019
Autoimmune Chronic Hepatitis
CUI: C0241910
Disease: Autoimmune Chronic Hepatitis
22 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.720 1.000 2 2014 2017
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
382 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.720 1.000 2 2019 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2145 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.710 1.000 1 2015 2016
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
995 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.710 1.000 1 2015 2016
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
233 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.710 1.000 1 2015 2018
Autoimmune hepatitis
CUI: C4721555
Disease: Autoimmune hepatitis
22 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.020 1.000 2 2014 2017
Diabetes
CUI: C0011847
Disease: Diabetes
611 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.020 0.500 2 2016 2017
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
714 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.020 0.500 2 2016 2017
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1000 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.020 1.000 2 2015 2019
Antiphospholipid Syndrome
CUI: C0085278
Disease: Antiphospholipid Syndrome
11 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.010 1.000 1 2013 2013
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.010 1.000 1 2016 2016
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.010 1.000 1 2018 2018
Eosinophilia
CUI: C0014457
Disease: Eosinophilia
22 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.010 1.000 1 2010 2010
Eosinophilic disorder
CUI: C1306759
Disease: Eosinophilic disorder
22 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.010 1.000 1 2010 2010
leukemia
CUI: C0023418
Disease: leukemia
138 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.010 1.000 1 2016 2016
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
2154 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.010 1.000 1 2015 2015
Malignant neoplasm of colon and/or rectum
502 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.010 1.000 1 2015 2015
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.010 1.000 1 2015 2015
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
448 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.010 1.000 1 2010 2010
Myeloid Leukemia, Chronic
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
95 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.010 1.000 1 2016 2016