rs113542380, THADA

N. diseases: 5
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.
Tonometry
CUI: C0040420
Disease: Tonometry
573 2 43237679 intron variant G/A snv 4.7E-02 0.700 1.000 3 2018 2018
Finding of Mean Corpuscular Hemoglobin
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
1206 2 43237679 intron variant G/A snv 4.7E-02 0.700 1.000 1 2016 2016
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 2 43237679 intron variant G/A snv 4.7E-02 0.700 1.000 1 2016 2016
Neutrophil count (procedure)
CUI: C0200633
Disease: Neutrophil count (procedure)
234 2 43237679 intron variant G/A snv 4.7E-02 0.700 1.000 1 2016 2016
Reticulocyte count (procedure)
CUI: C0206161
Disease: Reticulocyte count (procedure)
474 2 43237679 intron variant G/A snv 4.7E-02 0.700 1.000 1 2016 2016