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: rs12454712
rs12454712
0.925 0.120 18 63178651 intron variant T/A;C snv
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders
0.010 1.000 1 2010 2010
dbSNP: rs12454712
rs12454712
0.925 0.120 18 63178651 intron variant T/A;C snv
CUI: C0270549
Disease: Generalized Anxiety Disorder
Generalized Anxiety Disorder
0.010 1.000 1 2010 2010
dbSNP: rs12457893
rs12457893
1.000 0.080 18 63258928 intron variant A/C snv 0.39
CUI: C0022660
Disease: Kidney Failure, Acute
Kidney Failure, Acute
0.010 1.000 1 2012 2012
dbSNP: rs1310296388
rs1310296388
1.000 0.080 18 63318110 missense variant T/C snv 4.0E-06
Congenital Nonbullous Ichthyosiform Erythroderma
0.010 1.000 1 2009 2009
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: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.010 1.000 1 2013 2013
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: rs1564483
rs1564483
1.000 0.080 18 63127421 3 prime UTR variant C/T snv 0.22
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2012 2012
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: 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: C0279628
Disease: Adenocarcinoma Of Esophagus
Adenocarcinoma Of Esophagus
0.010 1.000 1 2011 2011
dbSNP: rs17757541
rs17757541
0.827 0.240 18 63212453 intron variant C/G;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 1.000 1 2016 2016
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: rs17759659
rs17759659
0.851 0.120 18 63291411 intron variant A/G snv 0.31
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease
0.010 1.000 1 2017 2017
dbSNP: rs17759659
rs17759659
0.851 0.120 18 63291411 intron variant A/G snv 0.31
CUI: C0018023
Disease: Nodular Goiter
Nodular Goiter
0.010 1.000 1 2017 2017
dbSNP: rs17759659
rs17759659
0.851 0.120 18 63291411 intron variant A/G snv 0.31
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis
0.010 1.000 1 2017 2017
dbSNP: rs17759659
rs17759659
0.851 0.120 18 63291411 intron variant A/G snv 0.31
CUI: C0151468
Disease: Thyroid Gland Follicular Adenoma
Thyroid Gland Follicular Adenoma
0.010 1.000 1 2017 2017
dbSNP: rs1800477
rs1800477
0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03
CUI: C0042769
Disease: Virus Diseases
Virus Diseases
0.010 1.000 1 2011 2011
dbSNP: rs1800477
rs1800477
0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03
CUI: C0004509
Disease: Azoospermia
Azoospermia
0.010 1.000 1 2010 2010
dbSNP: rs1800477
rs1800477
0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03
CUI: C0079731
Disease: B-Cell Lymphomas
B-Cell Lymphomas
0.010 1.000 1 2012 2012
dbSNP: rs1800477
rs1800477
0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs1800477
rs1800477
0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03
Diabetes Mellitus, Insulin-Dependent
0.010 < 0.001 1 2001 2001