SNP Report
                    
                        
                        Basic Info
                        
                     
                    
                        
                        
                                | Name | 
                                rs10949550 
                                    dbSNP
                                    Ensembl
                                 | 
                        
                        
                        
                                | Location | 
                                Chr6:18816997(Fwd) | 
                        
                        
                        
                        
                            | Variant Alleles | 
                            A/G | 
                        
                        
                        
                        
                            | Ancestral Allele | 
                            A | 
                        
                        
                        
                        
                            | No. of Studies | 
                            0 (significant: 0; non-significant: 0; trend: 0) | 
                        
                        
                            | Source | 
                            LD-proxy
 | 
                        
                    
                     
                    
                    
                        SNP related studies (count: 0)
                        
                     
                    
                    
                    
                        
                        SNP related genes (count: 0)
                        
                     
                    
                    
                    
                    
                        
                        
                        
                            
                                
                            
                            
                        
                        The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.
                    
                        
                            
                            Literature-origin SNPs (count: 1)
                            
                            
                        
                             | 
                            
                                | rs_ID | 
                                Functional Annotation | 
                                #studies(significant/non-significant/trend) | 
                                r2[population] | 
                            
                            
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | 
                                            rs41441749
                                         | 
                                         | 
                                        
                                            
                                                1(0/0/1)
                                            
                                         | 
                                        1.0[LWK]; 0.815[YRI]
 | 
                                        
                                
                            
                        
 
                            
                            
                        
                        
                            
                            
                                LD-proxies (count: 0)