Source: GWASDB

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: rs1897824
rs1897824
ZNF285B
1.000 0.080 19 44472854 non coding transcript exon variant T/A;C snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs2298428
rs2298428
YDJC
0.807 0.240 22 21628603 missense variant C/T snv 0.27 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs11089620
rs11089620
UBE2L3
1.000 0.080 22 21568167 non coding transcript exon variant C/G snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs12484550
rs12484550
UBE2L3
1.000 0.080 22 21587626 intron variant C/T snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs2256609
rs2256609
UBE2L3
0.925 0.080 22 21570728 intron variant A/G snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		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: C0019163
Disease: Hepatitis B
Hepatitis B 		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: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs2266963
rs2266963
UBE2L3
1.000 0.080 22 21593178 intron variant C/G snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs4821104
rs4821104
UBE2L3
1.000 0.080 22 21596116 intron variant A/G snv 0.19
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs4821114
rs4821114
UBE2L3
1.000 0.080 22 21616521 intron variant G/A;C snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
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: rs5749502
rs5749502
UBE2L3
1.000 0.080 22 21590807 intron variant T/A snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs5754166
rs5754166
UBE2L3
0.925 0.160 22 21576488 intron variant C/T snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs5754234
rs5754234
UBE2L3
1.000 0.080 22 21588689 intron variant A/T snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs5754344
rs5754344
UBE2L3
1.000 0.080 22 21609497 intron variant A/G snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs59391722
rs59391722
UBE2L3
1.000 0.080 22 21566528 intron variant G/C snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.710 1.000 1 2013 2019
dbSNP: rs73166619
rs73166619
UBE2L3
1.000 0.080 22 21575804 intron variant C/T snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs73166630
rs73166630
UBE2L3
1.000 0.080 22 21591689 intron variant G/A;T snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs9621715
rs9621715
UBE2L3
1.000 0.080 22 21587718 intron variant G/A snv 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs6141
rs6141
THPO
0.925 0.080 3 184372478 3 prime UTR variant C/G;T snv 4.0E-06; 0.56
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2011 2011
dbSNP: rs1419881
rs1419881
TCF19
0.851 0.280 6 31162816 3 prime UTR variant G/A snv 0.50
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.800 1.000 1 2013 2013
dbSNP: rs4148871
rs4148871
TAP2
0.925 0.080 6 32835539 intron variant A/G snv 0.82
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs4148876
rs4148876
TAP2
0.925 0.080 6 32829016 missense variant G/A snv 7.6E-02 5.7E-02
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs2253705
rs2253705
SFTA2
1.000 0.080 6 30932317 intron variant T/C snv 0.74
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs421446
rs421446
RING1 ; HSD17B8 ; MIR219A1
0.882 0.280 6 33207006 upstream gene variant A/G snv 0.32
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2011 2011