H19, imprinted maternally expressed transcript (non-protein coding)
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PharmGKB contains no Clinical Variants that meet the highest level of criteria.
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This is a non-comprehensive list of genetic tests with pharmacogenetics relevance, typically submitted by the manufacturer and manually curated by PharmGKB. The information listed is provided for educational purposes only and does not constitute an endorsement of any listed test or manufacturer.
A more complete listing of genetic tests is found at the Genetic Testing Registry (GTR).
|PGx Test||Variants Assayed||Related Drugs?|
|Alternate Names:||long intergenic non-protein coding RNA 8; non-protein coding RNA 8|
|Alternate Symbols: ||ASM; ASM1; D11S813E; LINC00008; NCRNA00008|
|PharmGKB Accession Id:||PA29091|
|Cytogenetic Location:||chr11 : p15.5 - p15.5|
|GP mRNA Boundary†:||chr11 : 2016406 - 2019065|
|GP Gene Boundary†:||chr11 : 2013406 - 2029065|
Publications related to H19: 1
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||Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype. American journal of human genetics. 2006. Bliek Jet, et al.|