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: rs3807306
rs3807306
0.776 0.320 7 128940626 intron variant G/A;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.800 1.000 2 2011 2012
dbSNP: rs3807307
rs3807307
0.827 0.120 7 128939148 intron variant T/C snv 0.41
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.800 1.000 1 2012 2012
dbSNP: rs7808907
rs7808907
1.000 0.080 7 128944030 intron variant T/C snv 0.49
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 2 2011 2014
dbSNP: rs3757387
rs3757387
0.851 0.280 7 128936032 upstream gene variant T/C snv 0.38
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs3778753
rs3778753
0.925 0.200 7 128939988 intron variant A/G snv 0.41
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs3778754
rs3778754
1.000 0.080 7 128935498 upstream gene variant C/G snv 0.40
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs3807306
rs3807306
0.776 0.320 7 128940626 intron variant G/A;T snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs3807306
rs3807306
0.776 0.320 7 128940626 intron variant G/A;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs3823536
rs3823536
0.925 0.280 7 128939612 intron variant G/A snv 0.40
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012