rs140570886, LPA

N. diseases: 3
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.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 1.000 0.040 6 160591981 intron variant T/C snv 2.8E-02 0.700 1.000 2 2017 2018
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 1.000 0.040 6 160591981 intron variant T/C snv 2.8E-02 0.700 1.000 1 2019 2019
Lipoprotein (a) measurement
CUI: C1096202
Disease: Lipoprotein (a) measurement
103 1.000 0.040 6 160591981 intron variant T/C snv 2.8E-02 0.700 1.000 1 2017 2017