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Ontology for Genetic Interval
Last uploaded:
August 20, 2015
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| Preferred Name | genetic polymorohism | |
| Synonyms |
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| Definitions |
strictly, the existense of two or more variants(alleles, phenotypes, sequence variants, chromosomal structural variants) at significant frequencies (i.e. more than 1%) in the population. Looser usages among molecular genetics include (1) any sequence variant present at a frequency >1% in a population (2) any non-pathogenic sequence variant, regardless of frequency. |
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| ID |
http://purl.obolibrary.org/obo/OGI_0000089 |
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| comment |
Looser usages among molecular genetics include (1) any sequence variant present at a frequency >1% in a population (2) any non-pathogenic sequence variant, regardless of frequency.
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| BFO_0000080 | ||
| definition |
strictly, the existense of two or more variants(alleles, phenotypes, sequence variants, chromosomal structural variants) at significant frequencies (i.e. more than 1%) in the population.
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| definition source |
http://purl.obolibrary.org/obo/OGI.owl#Human_Molecular_Genetics3 |
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| label |
genetic polymorohism
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| prefixIRI |
OGI:0000089
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| prefLabel |
genetic polymorohism
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| subClassOf |
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Create mapping
| Mapping To | Ontology | Source |
|---|---|---|
| http://purl.obolibrary.org/obo/OGI_0000089 | VDOT | SAME_URI |
| http://purl.obolibrary.org/obo/OGI_0000089 | OGSF | SAME_URI |
| http://purl.obolibrary.org/obo/OGI_0000089 | OGSF | LOOM |