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.
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.040 1.000 4 2015 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.040 1.000 4 2015 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.030 1.000 3 2015 2018
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.020 1.000 2 2013 2015
Malignant neoplasm of colon and/or rectum
502 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.020 1.000 2 2015 2018
Secondary malignant neoplasm of lymph node
188 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.020 0.500 2 2015 2018
Squamous cell carcinoma of esophagus
329 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.020 1.000 2 2014 2018
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1 2012 2012
Anal abscess
CUI: C0281778
Disease: Anal abscess
1 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1.000 1 2019 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1 2018 2018
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1.000 1 2018 2018
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1.000 1 2017 2017
Cervical Intraepithelial Neoplasia
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
29 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1.000 1 2017 2017
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1.000 1 2017 2017
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1.000 1 2016 2016
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1.000 1 2017 2017
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1 2019 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1.000 1 2019 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1 2018 2018
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1.000 1 2018 2018
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1.000 1 2017 2017
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1.000 1 2019 2019
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1.000 1 2016 2016
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1.000 1 2016 2016
Pulmonary arterial hypertension
CUI: C2973725
Disease: Pulmonary arterial hypertension
70 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 0.010 1.000 1 2017 2017