Source: GWASDB ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
253 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.800 1.000 3 2008 2016
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
109 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.800 1.000 2 2007 2010
Membranous glomerulonephritis
CUI: C0017665
Disease: Membranous glomerulonephritis
2 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.800 1.000 1 2011 2011
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
1613 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.700 1.000 3 2007 2011
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
166 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.700 1.000 2 2009 2012
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
80 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.700 1.000 1 2009 2009
Asthma
CUI: C0004096
Disease: Asthma
263 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.700 1.000 1 2011 2011
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
477 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.700 1.000 1 2007 2007
Immunoglobulin A measurement
CUI: C0202083
Disease: Immunoglobulin A measurement
5 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.700 1.000 1 2010 2010
Myasthenia Gravis
CUI: C0026896
Disease: Myasthenia Gravis
56 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.700 1.000 1 2012 2012