rs1805017, PLA2G7

N. diseases: 5
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 heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.851 0.240 6 46716485 missense variant C/A;T snv 4.0E-06; 0.31 0.040 1.000 4 2010 2018
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.851 0.240 6 46716485 missense variant C/A;T snv 4.0E-06; 0.31 0.010 1.000 1 2015 2015
Acute pancreatitis
CUI: C0001339
Disease: Acute pancreatitis
51 0.851 0.240 6 46716485 missense variant C/A;T snv 4.0E-06; 0.31 0.010 1.000 1 2017 2017
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.851 0.240 6 46716485 missense variant C/A;T snv 4.0E-06; 0.31 0.010 1.000 1 2017 2017
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.851 0.240 6 46716485 missense variant C/A;T snv 4.0E-06; 0.31 0.010 1 2017 2017