rs7028891, DELEC1

N. diseases: 2
Source: ALL
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.
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.925 0.280 9 114882735 intron variant A/G snv 0.50 0.700 1.000 1 2012 2012
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.925 0.280 9 114882735 intron variant A/G snv 0.50 0.010 1.000 1 2017 2017