rs10098310, CCDC26

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.
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
296 8 129601368 intron variant G/A;T snv 0.700 1.000 1 2011 2011
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
296 8 129601368 intron variant G/A;T snv 0.700 1.000 1 2011 2011
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 8 129601368 intron variant G/A;T snv 0.700 1.000 1 2011 2011