SNP Report
                    
                        
                        Basic Info
                        
                     
                    
                        
                        
                                | Name | 
                                rs62057071 
                                    dbSNP
                                    Ensembl
                                 | 
                        
                        
                                | Location | 
                                17:45782325 - 45782325(+) | 
                        
                        
                        
                            | Variant Seq | 
                            G | 
                        
                        
                        
                        
                            | Ancestral Allele | 
                            G | 
                        
                        
                        
                        
                            | Ref Seq | 
                            C | 
                        
                        
                        
                        
                            | Minor Allele Frequence | 
                            0.0860623 | 
                        
                        
                        
                        
                            | Annotation | 
                            
                                upstream_gene_variant; intron_variant; non_coding_transcript_variant
                             | 
                        
                        
                        
                        
                            | Variant Effect | 
                            
                                upstream_gene_variant(ENST00000582766, ENST00000347197, ENST00000293493, ENST00000352855, ENST00000619154, ENST00000339069, ENST00000398285, ENST00000577353, ENST00000314537); intron_variant(ENST00000587305, ENST00000634540); non_coding_transcript_variant(ENST00000587305)
                             | 
                        
                        
                        
                        
                            | SIFT Annotation | 
                            
                                deleterious; tolerated
                             | 
                        
                        
                        
                        
                            | SIFT Variant Effect | 
                            
                                deleterious(ENST00000430334); tolerated(ENST00000430334, ENST00000581448, ENST00000584420, ENST00000589780)
                             | 
                        
                        
                        
                        
                            | PolyPhen Annotation | 
                            
                                benign; possibly_damaging
                             | 
                        
                        
                        
                        
                            | PolyPhen Variant Effect | 
                            
                                benign(ENST00000430334, ENST00000581448, ENST00000584420, ENST00000589780); possibly_damaging(ENST00000430334, ENST00000584420)
                             | 
                        
                        
                        
                            | rSNP? | 
                            
                                
                                    
                                        
                                        Yes
                                        
                                        
                                    
                                    Link in rVarBase
                             | 
                        
                        
                            | Related Regulatory Elements | 
                            
                                n/a
                             | 
                        
                        
                            | Chromatin State | 
                            
                                Enhancers;Weak transcription;Bivalent Enhancer
                             | 
                        
                        
                            | No. of Marker's Association Results | 
                            0 (Positive: 0; Negative: 0; Trend: 0) | 
                        
                        
                            | Source | 
                            LD-proxy | 
                        
                    
                     
                    
                    
                        SNP related association results
                        
                     
                    
                    
                    
                    
                    
                        
                        SNP related genes (count: 1)
                        
                     
                    
                    
                    
                    
                    
                        
                        SNPs in LD with rs62057071 (count: 0)
                        
                     
                    
                        
                        
                        
                        SNP related eQTL (count: 1)