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    | Variant #0000681066 (NC_000017.10:g.78188134G>A, NC_000017.10(NM_000199.3):c.507-7C>T (SGSH))
        
          | Chromosome | 17 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Probably does not affect function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | likely benign |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.78188134G>A |  
          | DNA change (hg38) | - |  
          | Published as | SGSH(NM_000199.3):c.507-7C>T (p.(=)), SGSH(NM_001352921.1):c.507-7C>T |  
          | ISCN | - |  
          | DB-ID | SGSH_000103 See all 2 reported entries |  
          | Variant remarks | VKGL data sharing initiative Nederland |  
          | Reference | - |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | CLASSIFICATION record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | 0.00031 View details |  
          | Owner | VKGL-NL_Rotterdam |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Rotterdam |  
          | Date created | 2020-08-06 14:59:34 +02:00 (CEST) |  
          | Date last edited | 2022-11-01 13:01:21 +01:00 (CET) |   
 
 
 
       
 
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