|   
  
    | Variant #0000881552 (NC_000006.11:g.(132173376_132176065)_(132176164_132179807)del, NC_000006.11(NM_006208.2):c.(617+1_618-1)_(715+1_716-1)del (ENPP1))
        
          | Chromosome | 6 |  
          | Allele | Parent #1 |  
          | Affects function (as reported) | Affects function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | ACMG |  
          | Clinical classification | pathogenic (recessive) |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.(132173376_132176065)_(132176164_132179807)del |  
          | DNA change (hg38) | g.(131852236_131854925)_(131855024_131858667)del |  
          | Published as | del ex6 |  
          | ISCN | - |  
          | DB-ID | LAMA2_000000 See all 127 reported entries |  
          | Variant remarks | - |  
          | Reference | PubMed: Mercurio 2022, Journal: Mercurio 2022 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | SUMMARY record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | Johan den Dunnen |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Johan den Dunnen |  
          | Date created | 2022-10-23 14:20:36 +02:00 (CEST) |  
          | Date last edited | 2022-10-23 15:03:49 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
 |  
 
    Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
    Use our APIs  to retrieve data.
 |