Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3811444
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.800 1.000 2 2012 2018
dbSNP: rs3811444
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.800 1.000 1 2011 2011
dbSNP: rs3811444
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 3 2012 2019
dbSNP: rs3811444
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 2 2016 2017
dbSNP: rs3811444
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 2 2017 2019
dbSNP: rs3811444
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs3811444
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 2 2017 2019
dbSNP: rs3811444
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		0.700 1.000 1 2015 2015
dbSNP: rs3811444
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs3811444
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs3811444
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs3811444
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016