SELP, selectin P, 6403

N. diseases: 293; N. variants: 23
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: rs6131
rs6131 		0.851 0.200 1 169611647 missense variant C/T snv 0.20 0.22
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.030 1.000 3 2002 2016
dbSNP: rs6136
rs6136 		0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.020 1.000 2 2002 2014
dbSNP: rs6133
rs6133 		0.851 0.280 1 169596108 missense variant C/A;G snv 0.12
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs867479748
rs867479748 		0.925 0.160 1 169603047 missense variant C/T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2002 2002