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: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma 		0.030 1.000 3 2010 2015
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
Adult Diffuse Large B-Cell Lymphoma 		0.020 1.000 2 2010 2013
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin 		0.020 1.000 2 2007 2009
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0006271
Disease: Bronchiolitis
Bronchiolitis 		0.020 1.000 2 2017 2018
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0276447
Disease: Rhinovirus infection
Rhinovirus infection 		0.010 1.000 1 2018 2018
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C1302547
Disease: Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma 		0.010 1.000 1 2015 2015
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C1332979
Disease: Childhood Lymphoma
Childhood Lymphoma 		0.010 1.000 1 2008 2008
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0043144
Disease: Wheezing
Wheezing 		0.010 1.000 1 2017 2017
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2009 2009
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma 		0.010 1.000 1 2008 2008
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0220597
Disease: Adult Hodgkin Lymphoma
Adult Hodgkin Lymphoma 		0.010 1.000 1 2012 2012
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0334634
Disease: Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse
Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse 		0.010 1.000 1 2010 2010
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C1333064
Disease: Classical Hodgkin's Lymphoma
Classical Hodgkin's Lymphoma 		0.010 1.000 1 2013 2013
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2009 2009
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
Childhood Non-Hodgkin Lymphoma 		0.010 1.000 1 2009 2009
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.010 1.000 1 2018 2018
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0024419
Disease: Waldenstrom Macroglobulinemia
Waldenstrom Macroglobulinemia 		0.010 1.000 1 2009 2009
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.010 1.000 1 2012 2012
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
Adult Non-Hodgkin Lymphoma 		0.010 1.000 1 2009 2009
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2009 2009
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial 		0.010 1.000 1 2009 2009
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia 		0.010 1.000 1 2018 2018
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
Childhood Hodgkin Lymphoma 		0.010 1.000 1 2012 2012
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.010 1.000 1 2018 2018
dbSNP: rs1800890
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2009 2009