| Variant #0000879118 (NC_000021.8:g.46311813A>G, NM_000211.3:c.1323T>C (ITGB2))
        
          | Chromosome | 21 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Does not affect function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | benign |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.46311813A>G |  
          | DNA change (hg38) | g.44891898A>G |  
          | Published as | - |  
          | ISCN | - |  
          | DB-ID | ITGB2_000005 See all 5 reported entries |  
          | Variant remarks | - |  
          | Reference | PubMed: Van De Vijver 2012, Journal: Van De Vijver |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | SUMMARY record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | 0.67958 View details |  
          | Owner | Dirk Roos |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Johan den Dunnen |  
          | Date created | 2022-09-27 13:36:02 +02:00 (CEST) |  
          | Date last edited | N/A |   
 
 
 
       
 
 Variant on transcripts
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