rs2968478, None

N. diseases: 4
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.
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 16 88792238 intergenic variant T/G snv 0.61 0.700 1.000 1 2016 2016
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 16 88792238 intergenic variant T/G snv 0.61 0.700 1.000 1 2016 2016
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 16 88792238 intergenic variant T/G snv 0.61 0.700 1.000 1 2019 2019
Reticulocyte count (procedure)
CUI: C0206161
Disease: Reticulocyte count (procedure)
474 16 88792238 intergenic variant T/G snv 0.61 0.700 1.000 1 2016 2016