rs17342717, SLC17A1

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.
Finding of Mean Corpuscular Hemoglobin
1206 6 25821542 intron variant C/T snv 6.1E-02 0.800 1.000 2 2010 2012
Corpuscular Hemoglobin Concentration Mean
4389 6 25821542 intron variant C/T snv 6.1E-02 0.700 1.000 2 2010 2012
Ferritin measurement
CUI: C0373607
Disease: Ferritin measurement
21 6 25821542 intron variant C/T snv 6.1E-02 0.700 1.000 2 2011 2011
Serum ferritin measurement
CUI: C0696113
Disease: Serum ferritin measurement
21 6 25821542 intron variant C/T snv 6.1E-02 0.700 1.000 2 2011 2011
Iron level result
CUI: C0428578
Disease: Iron level result
16 6 25821542 intron variant C/T snv 6.1E-02 0.700 1.000 1 2011 2011
Iron measurement
CUI: C0337439
Disease: Iron measurement
16 6 25821542 intron variant C/T snv 6.1E-02 0.700 1.000 1 2011 2011
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 6 25821542 intron variant C/T snv 6.1E-02 0.700 1.000 1 2012 2012
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 6 25821542 intron variant C/T snv 6.1E-02 0.700 1.000 1 2009 2009