SNP Report
                    
                        
                        Basic Info
                        
 
                     
                    
                        
                        
                                | Name | rs56023973 
                                    dbSNP
                                    Ensembl | 
                        
                                | Location | 17:45840410 - 45840410(+) | 
                        
                        
                            | Variant Seq | T | 
                        
                        
                        
                            | Ancestral Allele | G | 
                        
                        
                        
                            | Ref Seq | G | 
                        
                        
                        
                            | Minor Allele Frequence | 0.0860623 | 
                        
                        
                        
                            | Annotation | downstream_gene_variant; upstream_gene_variant; intron_variant; non_coding_transcript_variant | 
                        
                        
                        
                            | Variant Effect | downstream_gene_variant(ENST00000314537, ENST00000619154, ENST00000535778, ENST00000634540, ENST00000581125, ENST00000579244, ENST00000339069, ENST00000293493, ENST00000347197, ENST00000398285, ENST00000579599); upstream_gene_variant(ENST00000329196); intron_variant(ENST00000634876); non_coding_transcript_variant(ENST00000634876) | 
                        
                        
                        
                            | SIFT Annotation | deleterious | 
                        
                        
                        
                            | SIFT Variant Effect | deleterious(ENST00000329196) | 
                        
                        
                        
                            | PolyPhen Annotation | probably_damaging | 
                        
                        
                        
                            | PolyPhen Variant Effect | probably_damaging(ENST00000329196) | 
                        
                        
                            | rSNP? | Yes
                                        
                                        
                                    
                                    Link in rVarBase | 
                        
                            | Related Regulatory Elements | Chromatin interactive region | 
                        
                            | Chromatin State | Weak transcription;Bivalent Enhancer;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: 3)
                        
 
                     
                    
                    
                    
                    
                    
                        
                        SNPs in LD with rs56023973 (count: 0)
                        
 
                     
                    
                        
                        
                        
                        SNP related eQTL (count: 1)
                        
