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.
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.070 1.000 7 2006 2018
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.070 0.714 7 2009 2019
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.070 0.714 7 2009 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.060 1.000 6 2007 2017
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.060 0.833 6 2010 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.060 1.000 6 2007 2017
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.050 1.000 5 2009 2017
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.040 1.000 4 2017 2018
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.040 1.000 4 2017 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.040 1.000 4 2014 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.040 0.750 4 2007 2018
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.040 1.000 4 2017 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.040 0.750 4 2007 2018
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.040 1.000 4 2018 2020
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.720 1.000 3 2012 2016
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2009 2018
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2009 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2007 2016
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2008 2014
Depressive Symptoms
CUI: C0086132
Disease: Depressive Symptoms
120 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2010 2016
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2011 2018
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2009 2018
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2012 2018
Acute GVH disease
CUI: C0856825
Disease: Acute GVH disease
49 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2012 2018
Adult Hodgkin Lymphoma
CUI: C0220597
Disease: Adult Hodgkin Lymphoma
27 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2013 2018