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: rs4821116
rs4821116
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
22 21577779 intron variant C/T snv 0.31
High density lipoprotein measurement
0.800 1.000 2 2010 2019
dbSNP: rs131654
rs131654
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
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: rs2266959
rs2266959
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 1 2012 2017
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: rs181362
rs181362
22 21577779 intron variant C/T snv 0.31
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2010 2013
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: 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: 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: 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: 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: 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: rs4820091
rs4820091
22 21585900 intron variant T/G snv 0.30
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
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: rs4821112
rs4821112
22 21610472 intron variant G/A snv 0.21
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases
0.700 1.000 1 2011 2011
dbSNP: rs4821112
rs4821112
22 21610472 intron variant G/A snv 0.21
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4821112
rs4821112
22 21610472 intron variant G/A snv 0.21
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.700 1.000 1 2011 2011
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
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: 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: rs5754217
rs5754217
0.925 0.120 22 21585386 intron variant G/T snv 0.31
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs5754217
rs5754217
0.925 0.120 22 21585386 intron variant G/T snv 0.31
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2013 2013
dbSNP: rs5754217
rs5754217
0.925 0.120 22 21585386 intron variant G/T snv 0.31
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.700 1.000 1 2011 2011
dbSNP: rs5754217
rs5754217
0.925 0.120 22 21585386 intron variant G/T snv 0.31
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 1 2008 2008