rs1905376, TRPS1

N. diseases: 2
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.
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 8 115521531 intron variant A/G snv 0.55 0.700 1.000 1 2016 2016
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1141 8 115521531 intron variant A/G snv 0.55 0.700 1.000 1 2016 2016