UBE2L3, ubiquitin conjugating enzyme E2 L3, 7332

N. diseases: 56; N. variants: 39
Disease: Hepatitis B ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4821116
rs4821116 		0.925 0.120 22 21619030 intron variant C/A;T snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.820 1.000 2 2013 2018
dbSNP: rs59391722
rs59391722 		1.000 0.080 22 21566528 intron variant G/C snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.710 1.000 2 2013 2019
dbSNP: rs11089620
rs11089620 		1.000 0.080 22 21568167 non coding transcript exon variant C/G snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs12484550
rs12484550 		1.000 0.080 22 21587626 intron variant C/T snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs2256609
rs2256609 		0.925 0.080 22 21570728 intron variant A/G snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs2266959
rs2266959 		0.776 0.200 22 21568615 intron variant G/T snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs2266961
rs2266961 		0.807 0.160 22 21574308 intron variant C/G snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs2266963
rs2266963 		1.000 0.080 22 21593178 intron variant C/G snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs4821104
rs4821104 		1.000 0.080 22 21596116 intron variant A/G snv 0.19
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs4821114
rs4821114 		1.000 0.080 22 21616521 intron variant G/A;C snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs5749502
rs5749502 		1.000 0.080 22 21590807 intron variant T/A snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs5754166
rs5754166 		0.925 0.160 22 21576488 intron variant C/T snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs5754234
rs5754234 		1.000 0.080 22 21588689 intron variant A/T snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs5754344
rs5754344 		1.000 0.080 22 21609497 intron variant A/G snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs73166619
rs73166619 		1.000 0.080 22 21575804 intron variant C/T snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs73166630
rs73166630 		1.000 0.080 22 21591689 intron variant G/A;T snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs9621715
rs9621715 		1.000 0.080 22 21587718 intron variant G/A snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013