SNP Report
                    
                        
                        Basic Info
                        
 
                     
                    
                        
                        
                                | Name | rs62055559 
                                    dbSNP
                                    Ensembl | 
                        
                                | Location | 17:45889772 - 45889772(+) | 
                        
                        
                            | Variant Seq | G | 
                        
                        
                        
                            | Ancestral Allele | T | 
                        
                        
                        
                            | Ref Seq | T | 
                        
                        
                        
                            | Minor Allele Frequence | 0.0856629 | 
                        
                        
                        
                            | Annotation | upstream_gene_variant; intron_variant; non_coding_transcript_variant | 
                        
                        
                        
                            | Variant Effect | upstream_gene_variant(ENST00000262410, ENST00000334239, ENST00000340799, ENST00000570299, ENST00000535772, ENST00000351559, ENST00000446361, ENST00000571311, ENST00000344290); intron_variant(ENST00000634876, ENST00000579244, ENST00000579599); non_coding_transcript_variant(ENST00000634876, ENST00000579244, ENST00000579599) | 
                        
                        
                        
                            | SIFT Annotation | tolerated | 
                        
                        
                        
                            | SIFT Variant Effect | tolerated(ENST00000329196) | 
                        
                        
                        
                            | PolyPhen Annotation | benign | 
                        
                        
                        
                            | PolyPhen Variant Effect | benign(ENST00000329196) | 
                        
                        
                            | rSNP? | Yes
                                        
                                        
                                    
                                    Link in rVarBase | 
                        
                            | Related Regulatory Elements | TF binding region;Chromatin interactive region | 
                        
                            | 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: 2)
                        
 
                     
                    
                    
                    
                    
                    
                        
                        SNPs in LD with rs62055559 (count: 0)
                        
 
                     
                    
                        
                        
                        
                        SNP related eQTL (count: 1)
                        
