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: rs4821116
rs4821116
UBE2L3
0.925 0.120 22 21619030 intron variant C/A;T snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.820 1.000 1 2013 2018
dbSNP: rs181362
rs181362
UBE2L3
22 21577779 intron variant C/T snv 0.31
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 4 2010 2019
dbSNP: rs2266959
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 2 2012 2017
dbSNP: rs131654
rs131654
UBE2L3
1.000 0.080 22 21562901 intron variant G/A;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.800 1.000 1 2009 2009
dbSNP: rs181359
rs181359
UBE2L3
0.882 0.080 22 21574352 intron variant G/A snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2010 2010
dbSNP: rs7444
rs7444
UBE2L3
1.000 0.080 22 21622645 3 prime UTR variant T/C snv 0.32
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 3 2015 2017
dbSNP: rs5754217
rs5754217
UBE2L3
0.925 0.120 22 21585386 intron variant G/T snv 0.31
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 2 2012 2017
dbSNP: rs7445
rs7445
UBE2L3
22 21622758 3 prime UTR variant C/G;T snv 0.22
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2018 2019
dbSNP: rs131656
rs131656
UBE2L3
22 21563161 intron variant G/A snv 0.20
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs131656
rs131656
UBE2L3
22 21563161 intron variant G/A snv 0.20
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs131656
rs131656
UBE2L3
22 21563161 intron variant G/A snv 0.20
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs131658
rs131658
UBE2L3
1.000 0.080 22 21563337 intron variant C/G snv 0.29
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2017 2017
dbSNP: rs138665726
rs138665726
UBE2L3
22 21563570 intron variant A/C snv 0.17
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016
dbSNP: rs138665726
rs138665726
UBE2L3
22 21563570 intron variant A/C snv 0.17
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs138665726
rs138665726
UBE2L3
22 21563570 intron variant A/C snv 0.17
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs181359
rs181359
UBE2L3
0.882 0.080 22 21574352 intron variant G/A snv 0.21
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris 		0.700 1.000 1 2015 2015
dbSNP: rs181360
rs181360
UBE2L3
22 21574627 intron variant T/G snv 0.21
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2017 2017
dbSNP: rs181362
rs181362
UBE2L3
22 21577779 intron variant C/T snv 0.31
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs2256609
rs2256609
UBE2L3
0.925 0.080 22 21570728 intron variant A/G snv 0.18
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2015 2015
dbSNP: rs2266959
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18
CUI: C0087031
Disease: Juvenile-Onset Still Disease
Juvenile-Onset Still Disease 		0.700 1.000 1 2013 2013
dbSNP: rs2266959
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2017 2017
dbSNP: rs2266959
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18
CUI: C1858558
Disease: Rheumatoid Arthritis, Systemic Juvenile
Rheumatoid Arthritis, Systemic Juvenile 		0.700 1.000 1 2013 2013
dbSNP: rs2266959
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18
CUI: C2931171
Disease: Juvenile pauciarticular chronic arthritis
Juvenile pauciarticular chronic arthritis 		0.700 1.000 1 2013 2013
dbSNP: rs2266959
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18
CUI: C1384600
Disease: Systemic onset juvenile chronic arthritis
Systemic onset juvenile chronic arthritis 		0.700 1.000 1 2013 2013
dbSNP: rs2266959
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18
CUI: C3898105
Disease: Oligoarticular Juvenile Idiopathic Arthritis
Oligoarticular Juvenile Idiopathic Arthritis 		0.700 1.000 1 2013 2013