Disease: Coronary Sclerosis, Medial, of Infancy ×
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: rs121918025
rs121918025 		0.925 0.080 6 131861704 missense variant G/T snv
CUI: C1859728
Disease: Coronary Sclerosis, Medial, of Infancy
Coronary Sclerosis, Medial, of Infancy 		Nutritional and Metabolic Diseases; Cardiovascular Diseases 0.700 0