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PharmGKB contains no Clinical Variants that meet the highest level of criteria.
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The annotations do not account for individual variations among patients, and cannot be considered inclusive of all proper methods of care or exclusive of other treatments. It remains the responsibility of the health-care provider to determine the best course of treatment for a patient. Adherence to any guideline is voluntary, with the ultimate determination regarding its application to be made solely by the clinician and the patient. PharmGKB assumes no responsibility for any injury or damage to persons or property arising out of or related to any use of the PharmGKB clinical annotations, or for any errors or omissions.
|Alternate Names:||AB-binding alcohol dehydrogenase; HADH2; MRXS10; mitochondrial RNase P subunit 2; short chain dehydrogenase/reductase family 5C, member 1; type 10 17b-HSD; type 10 17beta-hydroxysteroid dehydrogenase|
|Alternate Symbols: ||17b-HSD10; ABAD; CAMR; ERAB; MHBD; MRPP2; SDR5C1|
|PharmGKB Accession Id:||PA162391638|
|Cytogenetic Location:||chrX : p11.22 - p11.22|
|GP mRNA Boundary†:||chrX : 53458206 - 53461323|
|GP Gene Boundary†:||chrX : 53455206 - 53471323|
UCSC has a Genome Browser that you can use to view PharmGKB annotations for this gene in context with many other sources of information.View on UCSC Browser
Publications related to HSD17B10: 1
The following icons indicate that data of a certain type is available:
- DG Dosing Guideline information is available
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||Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation. American journal of human genetics. 2008. Froyen Guy, et al.|