Variant #0000000034 (NC_000011.9:g.5273541C>T)
      
      
        
          | Individual ID | 
          00000004, 00000005, 00000006, 00000011, 00000016, 00000018, 00000020, 00000023, 00000027, 00000032, 00000033, 00000035, 00000036, 00000042, 00000044, 00000045, 00000050, 00000054, 00000056, 00000063, 00000064, 00000066, 00000069, 00000072, 00000073, 00000074, 00000079, 00000080, 00000088, 00000090, 00000095, 00000099, 00000100, 00000109, 00000111, 00000112, 00000113, 00000114, 00000115, 00000120, 00000122, 00000123, 00000125, 00000130, 00000136, 00000137, 00000139, 00000142, 00000146, 00000147, 00000162, 00000163, 00000164, 00000170, 00000181, 00000184, 00000186, 00000201, 00000210, 00000212, 00000213, 00000214, 00000217, 00000221, 00000222, 00000231, 00000237, 00000238, 00000246, 00000247, 00000248, 00000249, 00000253, 00000255, 00000256, 00000260, 00000266, 00000272, 00000282, 00000293, 00000302, 00000315, 00000316, 00000317, 00000320 |  
        
          | Chromosome | 
          11 |  
        
          | Allele | 
          Parent #1 |  
        
          | Affects function (as reported) | 
          Affects function |  
        
          | Affects function (by curator) | 
          Not classified |  
        
          | Type | 
          Substitution |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.5273541C>T |  
        
          | Reference | 
          GenBank |  
        
          | DB-ID | 
          HBG1_000010 See all 2 reported entries |  
        
          | Frequency | 
          - |  
        
          | Variant remarks | 
          - |  
        
          | ClassClinical | 
          uncertain significance |  
        
          | 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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