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: rs3744935
rs3744935
0.882 0.080 18 63127447 3 prime UTR variant C/T snv 6.0E-03
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.010 1.000 1 2016 2016
dbSNP: rs3744935
rs3744935
0.882 0.080 18 63127447 3 prime UTR variant C/T snv 6.0E-03
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs4987856
rs4987856
0.925 0.120 18 63126261 3 prime UTR variant C/T snv 6.0E-02
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma
0.700 1.000 1 2016 2016
dbSNP: rs2279115
rs2279115
0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv
CUI: C0271055
Disease: Rhegmatogenous retinal detachment
Rhegmatogenous retinal detachment
0.020 1.000 2 2015 2017
dbSNP: rs4940576
rs4940576
0.925 0.040 18 63181406 intron variant T/A;C snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
0.700 1.000 2 2015 2017
dbSNP: rs4940576
rs4940576
0.925 0.040 18 63181406 intron variant T/A;C snv
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 2 2015 2017
dbSNP: rs1473418
rs1473418
1.000 0.080 18 63319316 5 prime UTR variant C/G snv 0.98
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
0.010 1.000 1 2015 2015
dbSNP: rs1473418
rs1473418
1.000 0.080 18 63319316 5 prime UTR variant C/G snv 0.98
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs1564483
rs1564483
1.000 0.080 18 63127421 3 prime UTR variant C/T snv 0.22
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2015 2015
dbSNP: rs1564483
rs1564483
1.000 0.080 18 63127421 3 prime UTR variant C/T snv 0.22
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2015 2015
dbSNP: rs17757541
rs17757541
0.827 0.240 18 63212453 intron variant C/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 1.000 1 2015 2015
dbSNP: rs17757541
rs17757541
0.827 0.240 18 63212453 intron variant C/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 1.000 1 2015 2015
dbSNP: rs17757541
rs17757541
0.827 0.240 18 63212453 intron variant C/G;T snv
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 1.000 1 2015 2015
dbSNP: rs2279115
rs2279115
0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs2279115
rs2279115
0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv
Squamous cell carcinoma of esophagus
0.010 1.000 1 2015 2015
dbSNP: rs2279115
rs2279115
0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv
CUI: C0242852
Disease: Proliferative vitreoretinopathy
Proliferative vitreoretinopathy
0.010 1.000 1 2015 2015
dbSNP: rs2279115
rs2279115
0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.060 1.000 6 2014 2017
dbSNP: rs2279115
rs2279115
0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.050 1.000 5 2014 2017
dbSNP: rs1800477
rs1800477
0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
0.010 1.000 1 2014 2014
dbSNP: rs7226979
rs7226979
0.925 0.120 18 63257737 intron variant C/T snv 0.42
CUI: C4021107
Disease: Non-obstructive azoospermia
Non-obstructive azoospermia
0.010 1.000 1 2014 2014
dbSNP: rs17757541
rs17757541
0.827 0.240 18 63212453 intron variant C/G;T snv
CUI: C0079731
Disease: B-Cell Lymphomas
B-Cell Lymphomas
0.020 1.000 2 2013 2015
dbSNP: rs4987856
rs4987856
0.925 0.120 18 63126261 3 prime UTR variant C/T snv 6.0E-02
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.800 1.000 2 2013 2016
dbSNP: rs1564483
rs1564483
1.000 0.080 18 63127421 3 prime UTR variant C/T snv 0.22
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs17757541
rs17757541
0.827 0.240 18 63212453 intron variant C/G;T snv
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma
0.010 1.000 1 2013 2013
dbSNP: rs4987852
rs4987852
0.925 0.120 18 63126688 3 prime UTR variant T/C snv 5.1E-02
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.800 1.000 1 2013 2013