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    | Variant #0000603923 (NC_000011.9:g.5222877_5250289del, NM_000518.4:c.-2038_*23951del (HBB))
        
          | Chromosome | 11 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Affects function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | pathogenic |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.5222877_5250289del |  
          | DNA change (hg38) | g.5201647_5229059del |  
          | Published as | Vietnamese, SE Asian (HPFH-7, SEA-HPFH), NC_000011.10:g.5201647-5229059del27412bp |  
          | ISCN | - |  
          | DB-ID | HBB_004012 |  
          | Variant remarks | HPFH, Hb F levels |  
          | Reference | IthaNet-1505 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | SUMMARY record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | IthaNet - Petros Kountouris |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Johan den Dunnen |  
          | Date created | 2019-11-08 15:46:08 +01:00 (CET) |  
          | Date last edited | N/A |   
 
 
 
       
 
 Variant on transcripts
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