rs218265, None

N. diseases: 10
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 4 54542832 intergenic variant T/C snv 0.21 0.700 1.000 2 2016 2017
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 4 54542832 intergenic variant T/C snv 0.21 0.700 1.000 2 2016 2017
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 4 54542832 intergenic variant T/C snv 0.21 0.700 1.000 2 2016 2017
Blood basophil count (lab test)
CUI: C0200641
Disease: Blood basophil count (lab test)
452 4 54542832 intergenic variant T/C snv 0.21 0.700 1.000 1 2016 2016
Corpuscular Hemoglobin Concentration Mean
4389 4 54542832 intergenic variant T/C snv 0.21 0.700 1.000 1 2012 2012
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 4 54542832 intergenic variant T/C snv 0.21 0.700 1.000 1 2016 2016
Granulocyte count
CUI: C0857490
Disease: Granulocyte count
150 4 54542832 intergenic variant T/C snv 0.21 0.700 1.000 1 2016 2016
Neutrophil count (procedure)
CUI: C0200633
Disease: Neutrophil count (procedure)
234 4 54542832 intergenic variant T/C snv 0.21 0.700 1.000 1 2016 2016
Reticulocyte count (procedure)
CUI: C0206161
Disease: Reticulocyte count (procedure)
474 4 54542832 intergenic variant T/C snv 0.21 0.700 1.000 1 2016 2016
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 4 54542832 intergenic variant T/C snv 0.21 0.700 1.000 1 2016 2016