rs12826786, None

N. diseases: 26
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 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.030 1.000 3 2017 2018
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.030 1.000 3 2015 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.030 1.000 3 2017 2018
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.020 1.000 2 2016 2017
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.020 0.500 2 2018 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.020 1.000 2 2016 2017
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.020 0.500 2 2018 2018
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.020 0.500 2 2017 2018
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.020 0.500 2 2018 2018
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.020 0.500 2 2017 2018
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1.000 1 2020 2020
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1.000 1 2017 2017
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1 2017 2017
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1.000 1 2018 2018
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1.000 1 2018 2018
Familial lichen amyloidosis
CUI: C0268398
Disease: Familial lichen amyloidosis
24 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1.000 1 2018 2018
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1.000 1 2016 2016
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1.000 1 2015 2015
Glioma
CUI: C0017638
Disease: Glioma
353 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1 2017 2017
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1.000 1 2017 2017
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1.000 1 2016 2016
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1.000 1 2018 2018
Pervasive Development Disorder
CUI: C0524528
Disease: Pervasive Development Disorder
49 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1.000 1 2020 2020
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1 2017 2017
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1.000 1 2017 2017