Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1050828
rs1050828
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 3 2013 2017
dbSNP: rs1050828
rs1050828
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 2 2013 2017
dbSNP: rs1050828
rs1050828
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02
Red cell distribution width determination
0.700 1.000 2 2013 2017
dbSNP: rs1050828
rs1050828
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 2 2013 2017
dbSNP: rs1050828
rs1050828
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02
RDW - Red blood cell distribution width result
0.700 1.000 2 2013 2017
dbSNP: rs1050828
rs1050828
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement
0.700 1.000 1 2017 2017