rs2075672, TFR2;ACTL6B

N. diseases: 8
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
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4389 7 100642673 intron variant A/G snv 0.65 0.800 1.000 2 2012 2016
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 7 100642673 intron variant A/G snv 0.65 0.700 1.000 3 2012 2017
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 7 100642673 intron variant A/G snv 0.65 0.700 1.000 1 2017 2017
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 7 100642673 intron variant A/G snv 0.65 0.700 1.000 1 2017 2017
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 7 100642673 intron variant A/G snv 0.65 0.700 1.000 1 2017 2017
Platelet Count measurement
CUI: C0032181
Disease: Platelet Count measurement
457 7 100642673 intron variant A/G snv 0.65 0.700 1.000 1 2016 2016
RDW - Red blood cell distribution width result
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
988 7 100642673 intron variant A/G snv 0.65 0.700 1.000 1 2019 2019
Red cell distribution width determination
CUI: C0427460
Disease: Red cell distribution width determination
988 7 100642673 intron variant A/G snv 0.65 0.700 1.000 1 2019 2019