rs112233623, CCND3

N. diseases: 5
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 41957260 intron variant C/T snv 7.0E-03 0.700 1.000 2 2016 2019
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 6 41957260 intron variant C/T snv 7.0E-03 0.700 1.000 2 2016 2016
RDW - Red blood cell distribution width result
988 6 41957260 intron variant C/T snv 7.0E-03 0.700 1.000 2 2016 2017
Red cell distribution width determination
988 6 41957260 intron variant C/T snv 7.0E-03 0.700 1.000 2 2016 2017
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 6 41957260 intron variant C/T snv 7.0E-03 0.700 1.000 1 2016 2016