Preferred Name (rdfs:label)

SNPO:observed_variation
ID

SNPO:observed_variation
Full Id

http://www.loria.fr/~coulet/ontology/snpontology/version1.5/snpontology_full.owl#observed_variation
comment

It is the variation (of nucleotides or of residues) observed between the 2 patients (reference sequence and the alternative sequence - if it's possible to talk about a "reference") when a genomic variation is described. Ex: A>C, CT>A, Ser>Thr, etc.
disjointWith

SNPO:variant

SNPO:sequence

SNPO:database

SNPO:sequence_position

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