rs507666, ABO

N. diseases: 8
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.
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 1.000 0.040 9 133273983 intron variant A/G snv 0.800 1.000 4 2013 2019
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 1.000 0.040 9 133273983 intron variant A/G snv 0.700 1.000 4 2013 2019
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 1.000 0.040 9 133273983 intron variant A/G snv 0.700 1.000 2 2018 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 1.000 0.040 9 133273983 intron variant A/G snv 0.700 1.000 2 2017 2018
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 1.000 0.040 9 133273983 intron variant A/G snv 0.700 1.000 1 2017 2017
E-selectin Measurement
CUI: C4722217
Disease: E-selectin Measurement
6 1.000 0.040 9 133273983 intron variant A/G snv 0.700 1.000 1 2017 2017
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 1.000 0.040 9 133273983 intron variant A/G snv 0.700 1.000 1 2012 2012
Venous Thrombosis
CUI: C0042487
Disease: Venous Thrombosis
218 1.000 0.040 9 133273983 intron variant A/G snv 0.700 1.000 1 2012 2012