SNP Report
                    
                        
                        Basic Info
                        
                     
                    
                        
                        
                                | Name | 
                                rs17690176 
                                    dbSNP
                                    Ensembl
                                 | 
                        
                        
                                | Location | 
                                17:45839407 - 45839407(+) | 
                        
                        
                        
                            | Variant Seq | 
                            C | 
                        
                        
                        
                        
                            | Ancestral Allele | 
                            C | 
                        
                        
                        
                        
                            | Ref Seq | 
                            A | 
                        
                        
                        
                        
                            | Minor Allele Frequence | 
                            0.086262 | 
                        
                        
                        
                        
                            | Annotation | 
                            
                                downstream_gene_variant; intron_variant; non_coding_transcript_variant
                             | 
                        
                        
                        
                        
                            | Variant Effect | 
                            
                                downstream_gene_variant(ENST00000634540, ENST00000339069, ENST00000293493, ENST00000577353, ENST00000535778, ENST00000352855, ENST00000398285, ENST00000579244, ENST00000619154, ENST00000581125, ENST00000347197, ENST00000314537, ENST00000583888, ENST00000580876, ENST00000579599); intron_variant(ENST00000634876); non_coding_transcript_variant(ENST00000634876)
                             | 
                        
                        
                        
                        
                            | SIFT Annotation | 
                            
                                deleterious
                             | 
                        
                        
                        
                        
                            | SIFT Variant Effect | 
                            
                                deleterious(ENST00000329196)
                             | 
                        
                        
                        
                        
                            | PolyPhen Annotation | 
                            
                                benign
                             | 
                        
                        
                        
                        
                            | PolyPhen Variant Effect | 
                            
                                benign(ENST00000329196)
                             | 
                        
                        
                        
                            | rSNP? | 
                            
                                
                                    
                                        
                                        Yes
                                        
                                        
                                    
                                    Link in rVarBase
                             | 
                        
                        
                            | Related Regulatory Elements | 
                            
                                Chromatin interactive region
                             | 
                        
                        
                            | Chromatin State | 
                            
                                Weak transcription;Enhancers
                             | 
                        
                        
                            | No. of Marker's Association Results | 
                            0 (Positive: 0; Negative: 0; Trend: 0) | 
                        
                        
                            | Source | 
                            LD-proxy | 
                        
                    
                     
                    
                    
                        SNP related association results
                        
                     
                    
                    
                    
                    
                    
                        
                        SNP related genes (count: 3)
                        
                     
                    
                    
                    
                    
                    
                        
                        SNPs in LD with rs17690176 (count: 0)
                        
                     
                    
                        
                        
                        
                        SNP related eQTL (count: 1)