Source: GWASCAT

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: rs2266959
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18
CUI: C3890205
Disease: Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative 		0.700 1.000 1 2013 2013
dbSNP: rs2266961
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs2266961
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs2266961
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs2266961
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs2266961
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs2266961
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs2283790
rs2283790
UBE2L3
0.882 0.120 22 21602364 intron variant A/G snv 0.21
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2017 2017
dbSNP: rs2283790
rs2283790
UBE2L3
0.882 0.120 22 21602364 intron variant A/G snv 0.21
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2017 2017
dbSNP: rs2283790
rs2283790
UBE2L3
0.882 0.120 22 21602364 intron variant A/G snv 0.21
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2013 2013
dbSNP: rs34977459
rs34977459
UBE2L3
22 21578365 intron variant AAAA/-;AA;AAA;AAAAA;AAAAAA;AAAAAAAAAAAA delins
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs374588807
rs374588807
UBE2L3
22 21584179 intron variant TTT/-;T;TT;TTTT;TTTTT delins 0.21
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2016 2016
dbSNP: rs4820091
rs4820091
UBE2L3
22 21585900 intron variant T/G snv 0.30
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2017 2017
dbSNP: rs4821112
rs4821112
UBE2L3
22 21610472 intron variant G/A snv 0.21
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2010 2010
dbSNP: rs4821116
rs4821116
UBE2L3
0.925 0.120 22 21619030 intron variant C/A;T snv 0.18
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2017 2017
dbSNP: rs530685161
rs530685161
UBE2L3
22 21597965 intron variant TTTTTTT/-;TTT;TTTT;TTTTT;TTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTTTT delins 0.22
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs5754100
rs5754100
UBE2L3
0.882 22 21561877 intron variant T/C snv 0.18
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs5754100
rs5754100
UBE2L3
0.882 22 21561877 intron variant T/C snv 0.18
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2019 2019
dbSNP: rs5754100
rs5754100
UBE2L3
0.882 22 21561877 intron variant T/C snv 0.18
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2019 2019
dbSNP: rs5754100
rs5754100
UBE2L3
0.882 22 21561877 intron variant T/C snv 0.18
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs5754100
rs5754100
UBE2L3
0.882 22 21561877 intron variant T/C snv 0.18
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2019 2019
dbSNP: rs5754102
rs5754102
UBE2L3
22 21561983 intron variant C/A snv 0.17
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs5754102
rs5754102
UBE2L3
22 21561983 intron variant C/A snv 0.17
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs5754166
rs5754166
UBE2L3
0.925 0.160 22 21576488 intron variant C/T snv 0.18
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs5754166
rs5754166
UBE2L3
0.925 0.160 22 21576488 intron variant C/T snv 0.18
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2019 2019