UTS2, urotensin 2, 10911

N. diseases: 115; N. variants: 7
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: rs201977733
rs201977733 		1.000 0.080 1 7850908 missense variant C/T snv 5.6E-05 2.1E-05
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2009 2009
dbSNP: rs2890565
rs2890565 		0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2009 2009