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Variant : CV455271 (Single allele) Homo sapiens

Symbol: CV455271
Name: Single allele
Condition: Parkinson disease 2 [RCV000559835]
Clinical Significance: pathogenic
Last Evaluated: 04/26/2018
Review Status: criteria provided, single submitter
Related Genes: PRKN  
Variant Type: deletion (SO:0000159)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh386162,262,505 - 162,262,785CLINVAR
Cytogenetic Map66q26CLINVAR
Trait Synonyms: Parkin Type of Early-Onset Parkinson Disease; Parkin Type of Juvenile Parkinson Disease

Disease Annotations
References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 13495730
Created: 2018-01-09
Species: Homo sapiens
Last Modified: 2019-11-12
Status: ACTIVE


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