rs9394841, CCND3

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
1206 6 41959197 intron variant T/C snv 0.22 0.700 1.000 1 2016 2016
RDW - Red blood cell distribution width result
988 6 41959197 intron variant T/C snv 0.22 0.700 1.000 1 2016 2016
Red cell distribution width determination
988 6 41959197 intron variant T/C snv 0.22 0.700 1.000 1 2016 2016