Variant #0000000070 (NC_000006.11:g.135426558A>T)
      
      
        
          | Individual ID | 
          00000001, 00000004, 00000007, 00000008, 00000018, 00000026, 00000031, 00000032, 00000033, 00000034, 00000036, 00000038, 00000039, 00000041, 00000043, 00000045, 00000050, 00000051, 00000053, 00000056, 00000065, 00000066, 00000068, 00000071, 00000072, 00000075, 00000079, 00000080, 00000081, 00000084, 00000089, 00000098, 00000100, 00000102, 00000103, 00000104, 00000105, 00000109, 00000110, 00000111, 00000119, 00000121, 00000122, 00000123, 00000126, 00000133, 00000136, 00000143, 00000147, 00000149, 00000151, 00000153, 00000156, 00000161, 00000162, 00000163, 00000165, 00000173, 00000174, 00000176, 00000177, 00000178, 00000179, 00000181, 00000182, 00000186, 00000188, 00000195, 00000200, 00000201, 00000206, 00000207, 00000214, 00000219, 00000222, 00000223, 00000226, 00000236, 00000240, 00000241, 00000243, 00000249, 00000251, 00000252, 00000263 |  
        
          | Chromosome | 
          6 |  
        
          | 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.135426558A>T |  
        
          | Reference | 
          GenBank;dbSNP |  
        
          | DB-ID | 
          HBS1L_000004 See all 3 reported entries |  
        
          | Frequency | 
          - |  
        
          | Variant remarks | 
          - |  
        
          | ClassClinical | 
          Likely benign |  
        
          | 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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