SNP Report
                    
                        
                        Basic Info
                        
 
                     
                    
                        
                        
                                | Name | rs17691610 
                                    dbSNP
                                    Ensembl | 
                        
                                | Location | 17:45893296 - 45893296(+) | 
                        
                        
                            | Variant Seq | T | 
                        
                        
                        
                            | Ancestral Allele | G | 
                        
                        
                        
                            | Ref Seq | G | 
                        
                        
                        
                            | Minor Allele Frequence | 0.0860623 | 
                        
                        
                        
                            | Annotation | upstream_gene_variant; intron_variant; non_coding_transcript_variant | 
                        
                        
                        
                            | Variant Effect | upstream_gene_variant(ENST00000334239, ENST00000571311, ENST00000340799, ENST00000344290, ENST00000624111, ENST00000535772, ENST00000446361, ENST00000570299, ENST00000351559, ENST00000262410); intron_variant(ENST00000634876, ENST00000579599, ENST00000579244); non_coding_transcript_variant(ENST00000634876, ENST00000579599, ENST00000579244) | 
                        
                        
                        
                            | 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;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: 4)
                        
 
                     
                    
                    
                    
                    
                    
                        
                        SNPs in LD with rs17691610 (count: 0)
                        
 
                     
                    
                        
                        
                        
                        SNP related eQTL (count: 1)
                        
