rs17476364, HK1

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.
Finding of Mean Corpuscular Hemoglobin
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
1206 10 69334748 intron variant T/C snv 6.4E-02 0.700 1.000 2 2016 2019
RDW - Red blood cell distribution width result
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
988 10 69334748 intron variant T/C snv 6.4E-02 0.700 1.000 2 2016 2019
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 10 69334748 intron variant T/C snv 6.4E-02 0.700 1.000 2 2016 2019
Red cell distribution width determination
CUI: C0427460
Disease: Red cell distribution width determination
988 10 69334748 intron variant T/C snv 6.4E-02 0.700 1.000 2 2016 2019
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 10 69334748 intron variant T/C snv 6.4E-02 0.700 1.000 1 2016 2016
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 10 69334748 intron variant T/C snv 6.4E-02 0.700 1.000 1 2016 2016
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 10 69334748 intron variant T/C snv 6.4E-02 0.700 1.000 1 2016 2016
Reticulocyte count (procedure)
CUI: C0206161
Disease: Reticulocyte count (procedure)
474 10 69334748 intron variant T/C snv 6.4E-02 0.700 1.000 1 2016 2016