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Variant : CV24904 (SYP, 4-BP DEL, 829GACT) Homo sapiens

Symbol: CV24904
Name: SYP, 4-BP DEL, 829GACT
Condition: Mental retardation, X-linked 96 [RCV000010540]
Clinical Significance: pathogenic
Last Evaluated: 02/17/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: SYP  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Nucleotide Change: 4-bp del, 829gact
Evidence: literature only
Position
Human AssemblyChrPosition (strand)Source
Cytogenetic MapXXp11.23-p11.22CLINVAR
Age Of Onset: childhood



Disease Annotations
References - curated
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 8561215
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.