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: rs1799945
rs1799945
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.840 1.000 1 2011 2019
dbSNP: rs1800562
rs1800562
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.800 1.000 3 2009 2012
dbSNP: rs1800562
rs1800562
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02
Low density lipoprotein cholesterol measurement
0.800 1.000 3 2010 2018
dbSNP: rs1800562
rs1800562
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 3 2010 2018
dbSNP: rs1799945
rs1799945
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10
Corpuscular Hemoglobin Concentration Mean
0.800 1.000 2 2012 2018
dbSNP: rs1800562
rs1800562
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02
Finding of Mean Corpuscular Hemoglobin
0.800 1.000 2 2010 2013
dbSNP: rs1800562
rs1800562
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.800 1.000 2 2009 2017
dbSNP: rs1799945
rs1799945
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.800 1.000 1 2009 2016
dbSNP: rs1800562
rs1800562
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.800 1.000 1 2009 2012
dbSNP: rs1800562
rs1800562
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
0.800 1.000 1 2011 2011
dbSNP: rs1799945
rs1799945
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 6 2011 2018
dbSNP: rs1799945
rs1799945
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 5 2011 2018
dbSNP: rs1799945
rs1799945
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement
0.700 1.000 2 2011 2017
dbSNP: rs1800562
rs1800562
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement
0.700 1.000 2 2011 2014
dbSNP: rs1800562
rs1800562
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02
Iron binding capacity total measurement
0.700 1.000 2 2011 2017
dbSNP: rs1800562
rs1800562
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement
0.700 1.000 2 2011 2014
dbSNP: rs1800562
rs1800562
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02
Total iron binding capacity function
0.700 1.000 2 2011 2017
dbSNP: rs1572982
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06
CUI: C0003467
Disease: Anxiety
Anxiety
0.700 1.000 1 2018 2018
dbSNP: rs1799945
rs1799945
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement
0.700 1.000 1 2017 2017
dbSNP: rs1799945
rs1799945
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10
RDW - Red blood cell distribution width result
0.700 1.000 1 2017 2017
dbSNP: rs1799945
rs1799945
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10
Red cell distribution width determination
0.700 1.000 1 2017 2017
dbSNP: rs1799945
rs1799945
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs1799945
rs1799945
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2018 2018
dbSNP: rs1799945
rs1799945
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs1799945
rs1799945
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement
0.700 1.000 1 2017 2017