rs6982502, None

N. diseases: 6
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.
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.882 0.080 8 125467120 intron variant C/T snv 0.62 0.700 1.000 1 2018 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.882 0.080 8 125467120 intron variant C/T snv 0.62 0.700 1.000 1 2018 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.882 0.080 8 125467120 intron variant C/T snv 0.62 0.700 1.000 1 2012 2012
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.882 0.080 8 125467120 intron variant C/T snv 0.62 0.700 1.000 1 2017 2017
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.882 0.080 8 125467120 intron variant C/T snv 0.62 0.700 1.000 1 2018 2018
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.882 0.080 8 125467120 intron variant C/T snv 0.62 0.010 1.000 1 2014 2014