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.
Vitiligo
CUI: C0042900
Disease: Vitiligo
121 0.827 0.280 6 32405921 intron variant G/A;T snv 0.800 1.000 2 2010 2012
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
1613 0.827 0.280 6 32405921 intron variant G/A;T snv 0.700 1.000 3 2007 2011
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
477 0.827 0.280 6 32405921 intron variant G/A;T snv 0.700 1.000 1 2007 2007
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
488 0.827 0.280 6 32405921 intron variant G/A;T snv 0.700 1.000 1 2007 2007
Narcolepsy
CUI: C0027404
Disease: Narcolepsy
436 0.827 0.280 6 32405921 intron variant G/A;T snv 0.700 1.000 1 2009 2009