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Variant : CV166588 (Single allele) Homo sapiens

Symbol: CV166588
Name: Single allele
Condition: Large for gestational age [RCV000161154]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: HNRNPCL1   PRAMEF11  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: case-control
Position
Human AssemblyChrPosition (strand)Source
GRCh37112,880,153 - 12,913,896CLINVAR
Cytogenetic Map11p36.21CLINVAR
Trait Synonyms: Birth weight > 90th percentile; Birthweight > 90th percentile; Fetal macrosomia; Macrosomia; Macrosomia, neonatal



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9831535
Created: 2015-03-10
Species: Homo sapiens
Last Modified: 2020-01-21
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.