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: rs582054
rs582054
0.882 0.160 3 159992214 intron variant A/C;T snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs582537
rs582537
1.000 0.080 3 159992311 intron variant A/C;G snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.800 1.000 1 2012 2017
dbSNP: rs586094
rs586094
1.000 0.080 3 160011761 non coding transcript exon variant T/G snv 0.41
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs587422
rs587422
1.000 0.080 3 160012018 non coding transcript exon variant G/A;C snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs600519
rs600519
1.000 0.080 3 160012630 intron variant G/A snv 0.41
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs629209
rs629209
1.000 0.080 3 160010926 intron variant C/G snv 0.41
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs6441286
rs6441286
0.925 0.080 3 160011091 intron variant T/G snv 0.36
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.800 1.000 2 2009 2010
dbSNP: rs6441288
rs6441288
1.000 0.080 3 160015053 intron variant C/T snv 0.41
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs647801
rs647801
1.000 0.080 3 159989732 intron variant A/G snv 0.58
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs669003
rs669003
1.000 0.080 3 160014098 intron variant A/G snv 0.41
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs6799788
rs6799788
1.000 0.040 3 159926508 intron variant A/G snv 0.18
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.800 1.000 1 2013 2013
dbSNP: rs6808024
rs6808024
1.000 0.080 3 159963878 intron variant A/T snv 0.12
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs76830965
rs76830965
0.925 0.120 3 159919889 intron variant C/A;G;T snv
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.700 1.000 1 2011 2011
dbSNP: rs9877910
rs9877910
1.000 0.080 3 160013032 intron variant C/T snv 0.36
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012