rs797044870, CDC42

N. diseases: 3
Disease: Multiple congenital anomalies ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Multiple congenital anomalies
CUI: C0000772
Disease: Multiple congenital anomalies
0.700 CausalMutation CLINVAR Rho GTPases and actin dynamics in membrane protrusions and vesicle trafficking. 16949823 2006
Multiple congenital anomalies
CUI: C0000772
Disease: Multiple congenital anomalies
0.700 CausalMutation CLINVAR Rho GTPases, dendritic structure, and mental retardation. 15884002 2005
Multiple congenital anomalies
CUI: C0000772
Disease: Multiple congenital anomalies
0.700 CausalMutation CLINVAR Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome. 12687501 2003
Multiple congenital anomalies
CUI: C0000772
Disease: Multiple congenital anomalies
0.700 CausalMutation CLINVAR GEFs and GAPs: critical elements in the control of small G proteins. 17540168 2007
Multiple congenital anomalies
CUI: C0000772
Disease: Multiple congenital anomalies
0.700 CausalMutation CLINVAR Differential localization of Rho GTPases in live cells: regulation by hypervariable regions and RhoGDI binding. 11149925 2001