rs1617640, EPO

N. diseases: 13
Source: BEFREE ×
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.
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
159 0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 0.040 0.750 4 2010 2017
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
188 0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 0.020 1.000 2 2008 2010
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
191 0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 0.020 1.000 2 2008 2010
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
CUI: C1845050
Disease: PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
36 0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 0.020 1.000 2 2008 2010
Anemia
CUI: C0002871
Disease: Anemia
79 0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 0.010 1.000 1 2015 2015
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 0.010 1.000 1 2012 2012
Early-Stage Breast Carcinoma
CUI: C2986665
Disease: Early-Stage Breast Carcinoma
7 0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 0.010 1.000 1 2012 2012
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
316 0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 0.010 1.000 1 2014 2014
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
131 0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 0.010 1 2015 2015
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
79 0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 0.010 1.000 1 2010 2010
Proliferative diabetic retinopathy
CUI: C0154830
Disease: Proliferative diabetic retinopathy
15 0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 0.010 1.000 1 2010 2010
Renal Insufficiency
CUI: C1565489
Disease: Renal Insufficiency
32 0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 0.010 1.000 1 2010 2010
Retinopathy of Prematurity
CUI: C0035344
Disease: Retinopathy of Prematurity
15 0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 0.010 1.000 1 2018 2018