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Variant : CV167128 (Single allele) Homo sapiens

Symbol: CV167128
Name: Single allele
Condition: Large for gestational age [RCV000161694]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: LINC00621  
Variant Type: duplication (SO:1000035)
Source: CLINVAR
Evidence: case-control
Position
Human AssemblyChrPosition (strand)Source
GRCh381322,782,997 - 22,941,414CLINVAR
GRCh371323,357,136 - 23,515,553CLINVAR
Cytogenetic Map1313q12.12CLINVAR
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: 9831929
Created: 2015-03-10
Species: Homo sapiens
Last Modified: 2020-01-14
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.