PLA2G7, phospholipase A2 group VII, 7941

N. diseases: 136; N. variants: 11
Disease: Myocardial Infarction ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1051931
rs1051931 		0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.040 1.000 4 2003 2011
dbSNP: rs13210554
rs13210554 		1.000 0.080 6 46736602 upstream gene variant C/T snv 0.20
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2009 2009
dbSNP: rs1805018
rs1805018 		0.827 0.200 6 46711566 missense variant A/G snv 6.8E-02 0.10
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2009 2009
dbSNP: rs76863441
rs76863441 		0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2009 2009