rs2413450, TMPRSS6

N. diseases: 5
Source: GWASCAT ×
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
1159 22 37074184 intron variant T/C snv 0.61 0.800 1.000 3 2009 2017
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 22 37074184 intron variant T/C snv 0.61 0.800 1.000 2 2009 2017
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
495 22 37074184 intron variant T/C snv 0.61 0.800 1.000 2 2009 2017
Corpuscular Hemoglobin Concentration Mean
165 22 37074184 intron variant T/C snv 0.61 0.800 1.000 1 2012 2017
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
209 22 37074184 intron variant T/C snv 0.61 0.800 1.000 1 2009 2017