rs9487023, CCDC162P

N. diseases: 8
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.
Corpuscular Hemoglobin Concentration Mean
4389 6 109268801 intron variant A/G snv 0.40 0.700 1.000 1 2016 2016
Finding of Mean Corpuscular Hemoglobin
1206 6 109268801 intron variant A/G snv 0.40 0.700 1.000 1 2016 2016
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 6 109268801 intron variant A/G snv 0.40 0.700 1.000 1 2016 2016
RDW - Red blood cell distribution width result
988 6 109268801 intron variant A/G snv 0.40 0.700 1.000 1 2017 2017
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 6 109268801 intron variant A/G snv 0.40 0.700 1.000 1 2016 2016
Red cell distribution width determination
988 6 109268801 intron variant A/G snv 0.40 0.700 1.000 1 2017 2017
Reticulocyte count (procedure)
CUI: C0206161
Disease: Reticulocyte count (procedure)
474 6 109268801 intron variant A/G snv 0.40 0.700 1.000 1 2016 2016
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 6 109268801 intron variant A/G snv 0.40 0.700 1.000 1 2019 2019