rs236918, PCSK7

N. diseases: 10
Source: ALL
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.
Soluble Transferrin Receptor Measurement
CUI: C3541318
Disease: Soluble Transferrin Receptor Measurement
7 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2011 2011
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 0.030 1.000 3 2014 2017
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 0.030 1.000 3 2014 2017
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 0.020 1.000 2 2016 2017
Hemochromatosis
CUI: C0018995
Disease: Hemochromatosis
45 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 0.010 1.000 1 2016 2016
HEMOCHROMATOSIS, TYPE 1
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
62 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 0.010 1.000 1 2016 2016
Hereditary hemochromatosis
CUI: C0392514
Disease: Hereditary hemochromatosis
56 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 0.010 1.000 1 2014 2014
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 0.010 1.000 1 2019 2019
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 0.010 1.000 1 2019 2019
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 0.010 1.000 1 2019 2019