Source: ALL

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: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2013 2013
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
Squamous cell carcinoma of esophagus
0.010 1.000 1 2013 2013
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2013 2013
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C1333064
Disease: Classical Hodgkin's Lymphoma
Classical Hodgkin's Lymphoma
0.010 1.000 1 2013 2013
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome
0.010 1.000 1 2013 2013
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
0.010 < 0.001 1 2013 2013
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
Drug-induced tardive dyskinesia
0.010 1.000 1 2013 2013
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
Squamous cell carcinoma of oropharynx
0.010 1.000 1 2013 2013
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.010 1.000 1 2013 2013
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.040 1.000 4 2012 2014
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
Diabetes Mellitus, Non-Insulin-Dependent
0.030 1.000 3 2010 2014
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0520575
Disease: Acute pyelonephritis
Acute pyelonephritis
0.010 1.000 1 2014 2014
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2014 2014
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2014 2014
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2014 2014
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0333184
Disease: Calcific stenosis
Calcific stenosis
0.010 1.000 1 2014 2014
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2014 2014
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 1.000 1 2014 2014
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0343640
Disease: African Burkitt's lymphoma
African Burkitt's lymphoma
0.010 1.000 1 2014 2014
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.020 1.000 2 2007 2015
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal
0.010 1.000 1 2015 2015
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
Liver and Intrahepatic Biliary Tract Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0085695
Disease: Chronic gastritis
Chronic gastritis
0.010 1.000 1 2015 2015
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0343641
Disease: Human papilloma virus infection
Human papilloma virus infection
0.010 1.000 1 2015 2015