rs17076726, CPEB4

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.
Finding of Mean Corpuscular Hemoglobin
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
1206 5 173936886 intron variant C/T snv 0.43 0.700 1.000 1 2016 2016
RDW - Red blood cell distribution width result
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
988 5 173936886 intron variant C/T snv 0.43 0.700 1.000 1 2016 2016
Red cell distribution width determination
CUI: C0427460
Disease: Red cell distribution width determination
988 5 173936886 intron variant C/T snv 0.43 0.700 1.000 1 2016 2016