SNP Report
                    
                        
                        Basic Info
                        
 
                     
                    
                        
                        
                                | Name | rs28716779 
                                    dbSNP
                                    Ensembl | 
                        
                                | Location | 15:61193099 - 61193099(+) | 
                        
                        
                            | Variant Seq | A | 
                        
                        
                        
                            | Ancestral Allele | G | 
                        
                        
                        
                            | Ref Seq | G | 
                        
                        
                        
                            | Minor Allele Frequence | 0.207668 | 
                        
                        
                        
                            | Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant | 
                        
                        
                        
                            | Variant Effect | intron_variant(ENST00000561093, ENST00000560876, ENST00000558904, ENST00000557822, ENST00000335670, ENST00000551975, ENST00000559145, ENST00000560300); NMD_transcript_variant(ENST00000551975); non_coding_transcript_variant(ENST00000561093, ENST00000560876, ENST00000557822, ENST00000559145, ENST00000560300) | 
                        
                        
                        
                            | SIFT Annotation | deleterious_-_low_confidence; tolerated | 
                        
                        
                        
                            | SIFT Variant Effect | deleterious_-_low_confidence(ENST00000551975); tolerated(ENST00000335670) | 
                        
                        
                        
                            | PolyPhen Annotation | benign; possibly_damaging | 
                        
                        
                        
                            | PolyPhen Variant Effect | benign(ENST00000335670); possibly_damaging(ENST00000551975) | 
                        
                        
                            | rSNP? | Yes
                                        
                                        
                                    
                                    Link in rVarBase | 
                        
                            | Related Regulatory Elements | n/a | 
                        
                            | Chromatin State | Weak transcription | 
                        
                            | 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 rs28716779 (count: 0)
                        
 
                     
                    
                        
                        
                        
                        SNP related eQTL (count: 1)
                        
