As of 2022-03-07, the Wikidata property ClinVar Variation ID (P1929) is used on 3 items as main value on statements (not counting qualifiers) of the Q and P namespaces.

Closest properties: by cardinality of intersection, by Jaccard index.

Display properties of the following types:                                    

Closest properties by cardinality of intersection

IDLabelIntersection cardinalityJaccard index
P6861 dbSNP ID 3
 0.1667
P3331 HGVS nomenclature 3
 0.0032
P31 instance of 3
 0.0000
P3433 biological variant of 2
 0.0010
P1057 chromosome 2
 0.0000
P644 genomic start 2
 0.0000
P645 genomic end 2
 0.0000
P1199 mode of inheritance 1
 0.0116
P3356 positive diagnostic predictor 1
 0.0075
P3359 negative prognostic predictor 1
 0.0050
P3355 negative therapeutic predictor 1
 0.0021
P3354 positive therapeutic predictor 1
 0.0018
P3329 CIViC variant ID 1
 0.0005
P1542 has effect 1
 0.0002
P10283 OpenAlex ID 1
 0.0000
P704 Ensembl transcript ID 1
 0.0000
P1050 medical condition 1
 0.0000
P6366 Microsoft Academic ID 1
 0.0000
P1343 described by source 1
 0.0000
P688 encodes 1
 0.0000
P856 official website 1
 0.0000
P2671 Google Knowledge Graph ID 1
 0.0000

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P6861 dbSNP ID 3
 0.1667
P1199 mode of inheritance 1
 0.0116
P3356 positive diagnostic predictor 1
 0.0075
P3359 negative prognostic predictor 1
 0.0050
P3331 HGVS nomenclature 3
 0.0032
P3355 negative therapeutic predictor 1
 0.0021
P3354 positive therapeutic predictor 1
 0.0018
P3433 biological variant of 2
 0.0010
P3329 CIViC variant ID 1
 0.0005
P1542 has effect 1
 0.0002
P10283 OpenAlex ID 1
 0.0000
P704 Ensembl transcript ID 1
 0.0000
P1050 medical condition 1
 0.0000
P6366 Microsoft Academic ID 1
 0.0000
P1057 chromosome 2
 0.0000
P644 genomic start 2
 0.0000
P645 genomic end 2
 0.0000
P1343 described by source 1
 0.0000
P688 encodes 1
 0.0000
P856 official website 1
 0.0000
P2671 Google Knowledge Graph ID 1
 0.0000
P31 instance of 3
 0.0000