rs3811444, TRIM58

N. diseases: 12
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 1 247876149 missense variant C/T snv 0.31 0.26 0.800 1.000 3 2012 2018
Platelet Count measurement
CUI: C0032181
Disease: Platelet Count measurement
457 1 247876149 missense variant C/T snv 0.31 0.26 0.800 1.000 1 2011 2011
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 1 247876149 missense variant C/T snv 0.31 0.26 0.700 1.000 3 2012 2019
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 1 247876149 missense variant C/T snv 0.31 0.26 0.700 1.000 2 2016 2017
RDW - Red blood cell distribution width result
988 1 247876149 missense variant C/T snv 0.31 0.26 0.700 1.000 2 2017 2019
Red cell distribution width determination
988 1 247876149 missense variant C/T snv 0.31 0.26 0.700 1.000 2 2017 2019
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 1 247876149 missense variant C/T snv 0.31 0.26 0.700 1.000 2 2016 2019
Fatty acid measurement
CUI: C1281901
Disease: Fatty acid measurement
116 1 247876149 missense variant C/T snv 0.31 0.26 0.700 1.000 1 2015 2015
Finding of Mean Corpuscular Hemoglobin
1206 1 247876149 missense variant C/T snv 0.31 0.26 0.700 1.000 1 2019 2019
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 1 247876149 missense variant C/T snv 0.31 0.26 0.700 1.000 1 2016 2016
Platelet mean volume determination (procedure)
371 1 247876149 missense variant C/T snv 0.31 0.26 0.700 1.000 1 2016 2016
Reticulocyte count (procedure)
CUI: C0206161
Disease: Reticulocyte count (procedure)
474 1 247876149 missense variant C/T snv 0.31 0.26 0.700 1.000 1 2016 2016