Variant #0000000388 (NC_000011.9:g.5248159C>A, HBB(NM_000518.4):c.92+1G>T)
      
      
        
          | Individual ID | 
          00000017, 00000738 |  
        
          | Chromosome | 
          11 |  
        
          | Allele | 
          Both (homozygous) |  
        
          | Affects function (as reported) | 
          Affects function |  
        
          | Affects function (by curator) | 
          Not classified |  
        
          | Type | 
          Substitution |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.5248159C>A |  
        
          | Reference | 
          (OMIM 0347);dbSNP;Chen et al. |  
        
          | DB-ID | 
          HBB_000058 See all 2 reported entries |  
        
          | Frequency | 
          - |  
        
          | Variant remarks | 
          IVS-I-1 (G->T) |  
        
          | ClassClinical | 
          Pathogenic |  
        
          | Average frequency (gnomAD v.2.1.1) | 
          Retrieve |  
        
          | Owner | 
          Qi Ming |  
        
          | Database submission license | 
          No license selected |  
        
          | Created by | 
          Qi Ming |   
        
      
      
      
  
      
       
      
  
      Variant on transcripts
      
      
       
      
      
  
      Screenings
       
      
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