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Variant : CV26195 (CHM, L1 INS) Homo sapiens

Symbol: CV26195
Name: CHM, L1 INS
Condition: Choroideremia [RCV000011906]
Clinical Significance: pathogenic
Last Evaluated: 11/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CHM  
Variant Type: insertion (SO:0000667)
Source: CLINVAR
Evidence: literature only
Position
Human AssemblyChrPosition (strand)Source
Cytogenetic MapXXq21.2CLINVAR
Age Of Onset: adolescence / young adulthood|adolescent|childhood
Prevalence: 1-9 / 100 000



Disease Annotations
References - curated
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 8562216
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2019-09-10
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.