rs1505307, THRB

N. diseases: 7
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 3 24301839 intron variant T/C snv 0.60 0.700 1.000 2 2017 2018
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 3 24301839 intron variant T/C snv 0.60 0.700 1.000 2 2017 2018
RDW - Red blood cell distribution width result
988 3 24301839 intron variant T/C snv 0.60 0.700 1.000 2 2016 2019
Red cell distribution width determination
988 3 24301839 intron variant T/C snv 0.60 0.700 1.000 2 2016 2019
Corpuscular Hemoglobin Concentration Mean
4389 3 24301839 intron variant T/C snv 0.60 0.700 1.000 1 2012 2012
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 3 24301839 intron variant T/C snv 0.60 0.700 1.000 1 2018 2018
Reticulocyte count (procedure)
CUI: C0206161
Disease: Reticulocyte count (procedure)
474 3 24301839 intron variant T/C snv 0.60 0.700 1.000 1 2016 2016