rs12935413, CLEC16A

N. diseases: 3
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 1.000 0.080 16 11116590 intron variant G/A snv 0.34 0.700 1.000 2 2011 2012
Blood basophil count (lab test)
CUI: C0200641
Disease: Blood basophil count (lab test)
452 1.000 0.080 16 11116590 intron variant G/A snv 0.34 0.700 1.000 1 2016 2016
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 1.000 0.080 16 11116590 intron variant G/A snv 0.34 0.700 1.000 1 2016 2016