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: rs12649554
rs12649554
1.000 0.080 4 100975519 regulatory region variant T/C snv 0.65
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.700 1.000 1 2011 2011
dbSNP: rs17401966
rs17401966
0.790 0.280 1 10325413 intron variant A/G snv 0.24
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.730 0.750 1 2011 2019
dbSNP: rs739496
rs739496
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.700 1.000 1 2011 2011
dbSNP: rs3782886
rs3782886
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.700 1.000 1 2011 2011
dbSNP: rs671
rs671
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.710 1.000 1 2011 2019
dbSNP: rs7775698
rs7775698
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.700 1.000 1 2011 2011
dbSNP: rs555627
rs555627
1.000 0.080 6 159538641 intron variant G/A snv 7.6E-02
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.700 1.000 1 2013 2013
dbSNP: rs17056316
rs17056316
1.000 0.080 4 170892334 downstream gene variant A/G snv 2.6E-03
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.700 1.000 1 2013 2013
dbSNP: rs6141
rs6141
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: rs59391722
rs59391722
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: 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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
0.700 1.000 1 2013 2013