Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.030 1.000 3 2015 2017
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.030 1.000 3 2017 2018
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.030 1.000 3 2017 2018
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.020 1.000 2 2016 2017
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.020 0.500 2 2017 2018
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.020 0.500 2 2017 2018
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.020 0.500 2 2018 2018
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.020 0.500 2 2018 2018
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.020 0.500 2 2018 2018
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.020 1.000 2 2016 2017
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0268398
Disease: Familial lichen amyloidosis
Familial lichen amyloidosis 		0.010 1.000 1 2018 2018
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids 		0.010 1.000 1 2019 2019
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia 		0.010 1.000 1 2017 2017
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma 		0.010 1.000 1 2018 2018
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma 		0.010 1.000 1 2018 2018
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2017 2017
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 < 0.001 1 2017 2017
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.010 1.000 1 2020 2020
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		0.010 1.000 1 2016 2016
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0017638
Disease: Glioma
Glioma 		0.010 < 0.001 1 2017 2017
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		0.010 1.000 1 2018 2018
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis 		0.010 1.000 1 2015 2015
dbSNP: rs12826786
rs12826786 		0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.010 < 0.001 1 2017 2017