rs4970966, ENSA

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.
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
296 1 150611627 intron variant G/T snv 0.16 0.700 1.000 2 2016 2018
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
296 1 150611627 intron variant G/T snv 0.16 0.700 1.000 2 2016 2018