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: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2013 2013
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C0280100
Disease: Solid Neoplasm
Solid Neoplasm
0.010 1.000 1 2013 2013
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C0018099
Disease: Gout
Gout
0.010 1.000 1 2015 2015
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
0.010 1.000 1 2012 2012
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C0023895
Disease: Liver diseases
Liver diseases
0.010 1.000 1 2013 2013
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
Squamous cell carcinoma of esophagus
0.010 1.000 1 2014 2014
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.010 1.000 1 2020 2020
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C0035439
Disease: Rheumatic Heart Disease
Rheumatic Heart Disease
0.010 < 0.001 1 2018 2018
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.010 < 0.001 1 2016 2016
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome
0.010 1.000 1 2009 2009
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 < 0.001 1 2008 2008
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2012 2012
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C0398650
Disease: Immune thrombocytopenic purpura
Immune thrombocytopenic purpura
0.010 1.000 1 2013 2013
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
Secondary malignant neoplasm of lymph node
0.010 1.000 1 2012 2012
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2012 2012
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C0013537
Disease: Eclampsia
Eclampsia
0.010 1.000 1 2019 2019
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis Syndrome
0.010 1.000 1 2019 2019
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
Diabetes Mellitus, Insulin-Dependent
0.010 < 0.001 1 2013 2013
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2019 2019
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
0.010 1.000 1 2009 2009
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
Necrotizing enterocolitis in fetus OR newborn
0.010 < 0.001 1 2017 2017
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2012 2012