PROKR1, prokineticin receptor 1, 10887

N. diseases: 27; N. variants: 3
Disease: Hirschsprung Disease ×
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: rs144018404
rs144018404 		1.000 0.080 2 68655413 missense variant T/A snv 5.6E-04 6.2E-04
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases 0.700 0