rs17534202, None

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.
RDW - Red blood cell distribution width result
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
988 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 0.700 1.000 3 2016 2019
Red cell distribution width determination
CUI: C0427460
Disease: Red cell distribution width determination
988 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 0.700 1.000 3 2016 2019
Finding of Mean Corpuscular Hemoglobin
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
1206 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 0.700 1.000 2 2016 2019
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 0.700 1.000 2 2016 2019
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 0.700 1.000 1 2016 2016
Reticulocyte count (procedure)
CUI: C0206161
Disease: Reticulocyte count (procedure)
474 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 0.700 1.000 1 2016 2016
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 0.010 1.000 1 2014 2014