SNP Report
                    
                        
                        Basic Info
                        
 
                     
                    
                        
                        
                                | Name | rs61882461 
                                    dbSNP
                                    Ensembl | 
                        
                                | Location | 11:17995580 - 17995580(+) | 
                        
                        
                            | Variant Seq | C | 
                        
                        
                        
                            | Ancestral Allele | T | 
                        
                        
                        
                            | Ref Seq | T | 
                        
                        
                        
                            | Minor Allele Frequence | 0.102236 | 
                        
                        
                        
                            | Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant | 
                        
                        
                        
                            | Variant Effect | downstream_gene_variant(ENST00000525523, ENST00000532212, ENST00000524716); intron_variant(ENST00000532265, ENST00000529728, ENST00000525422, ENST00000530613, ENST00000530925, ENST00000533328, ENST00000528200, ENST00000525920, ENST00000527494, ENST00000532546, ENST00000532389, ENST00000529151, ENST00000265965, ENST00000529440); NMD_transcript_variant(ENST00000525422, ENST00000530925, ENST00000533328, ENST00000527494, ENST00000532546); non_coding_transcript_variant(ENST00000529440) | 
                        
                        
                        
                            | SIFT Annotation | tolerated | 
                        
                        
                        
                            | SIFT Variant Effect | tolerated(ENST00000525920, ENST00000530613, ENST00000529728, ENST00000532389, ENST00000265965, ENST00000528200, ENST00000532265, ENST00000529151, ENST00000525422) | 
                        
                        
                        
                            | PolyPhen Annotation | benign | 
                        
                        
                        
                            | PolyPhen Variant Effect | benign(ENST00000525920, ENST00000530613, ENST00000529728, ENST00000532389, ENST00000265965, ENST00000528200, ENST00000532265, ENST00000529151, ENST00000525422) | 
                        
                        
                            | rSNP? | Yes
                                        
                                        
                                    
                                    Link in rVarBase | 
                        
                            | Related Regulatory Elements | n/a | 
                        
                            | Chromatin State | Weak transcription;Strong transcription;Genic 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: 1)
                        
 
                     
                    
                    
                    
                    
                    
                        
                        SNPs in LD with rs61882461 (count: 0)
                        
 
                     
                    
                        
                        
                        
                        SNP related eQTL (count: 1)
                        
