Source: ALL
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.
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.070 1.000 7 2003 2016
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.070 0.571 7 2002 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.060 1.000 6 2006 2015
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.060 1.000 6 2002 2014
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.060 1.000 6 2001 2009
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
81 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.060 1.000 6 1998 2012
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.060 1.000 6 2006 2015
Cooley's anemia
CUI: C0002875
Disease: Cooley's anemia
19 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.050 1.000 5 2000 2019
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
95 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.050 1.000 5 2003 2015
Alcoholic Liver Diseases
CUI: C0023896
Disease: Alcoholic Liver Diseases
20 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.040 1.000 4 1999 2003
Arthropathy
CUI: C0022408
Disease: Arthropathy
10 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.040 1.000 4 2006 2014
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.040 1.000 4 2002 2018
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.040 1.000 4 2001 2011
HFE-Associated Hereditary Hemochromatosis
CUI: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
3 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.040 1.000 4 2002 2014
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.800 1.000 4 2009 2012
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.030 1.000 3 2002 2013
Anemia, Hemolytic
CUI: C0002878
Disease: Anemia, Hemolytic
31 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.030 1.000 3 1998 2009
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.030 1.000 3 2000 2008
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.030 1.000 3 2000 2008
beta Thalassemia
CUI: C0005283
Disease: beta Thalassemia
103 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.030 1.000 3 2005 2017
beta^+^ Thalassemia
CUI: C3841475
Disease: beta^+^ Thalassemia
44 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.030 1.000 3 2005 2017
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.030 1.000 3 2001 2008
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.030 1.000 3 2002 2014
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.030 1.000 3 2002 2006
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.030 1.000 3 2003 2018