As of 2022-03-07, the Wikidata property biological variant of (P3433) is used on 2,077 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
P3329 CIViC variant ID 1,963
 0.9451
P31 instance of 1,766
 0.0000
P644 genomic start 1,427
 0.0014
P645 genomic end 1,427
 0.0014
P1057 chromosome 1,426
 0.0023
P3331 HGVS nomenclature 926
 0.4454
P3354 positive therapeutic predictor 569
 0.2740
P3355 negative therapeutic predictor 466
 0.2244
P3359 negative prognostic predictor 198
 0.0953
P3356 positive diagnostic predictor 132
 0.0636
P279 subclass of 87
 0.0000
P3358 positive prognostic predictor 70
 0.0337
P703 found in taxon 20
 0.0000
P3357 negative diagnostic predictor 9
 0.0043
P2671 Google Knowledge Graph ID 7
 0.0000
P6861 dbSNP ID 3
 0.0014
P10283 OpenAlex ID 3
 0.0000
P6366 Microsoft Academic ID 3
 0.0000
P1929 ClinVar Variation ID 2
 0.0010
P1449 nickname 2
 0.0001
P18 image 2
 0.0000
P1199 mode of inheritance 1
 0.0005
P10376 ScienceDirect topic ID 1
 0.0003
P1542 has effect 1
 0.0002
P1269 facet of 1
 0.0000
P704 Ensembl transcript ID 1
 0.0000
P1050 medical condition 1
 0.0000
P1889 different from 1
 0.0000
P1343 described by source 1
 0.0000
P361 part of 1
 0.0000
P646 Freebase ID 1
 0.0000

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P3329 CIViC variant ID 1,963
 0.9451
P3331 HGVS nomenclature 926
 0.4454
P3354 positive therapeutic predictor 569
 0.2740
P3355 negative therapeutic predictor 466
 0.2244
P3359 negative prognostic predictor 198
 0.0953
P3356 positive diagnostic predictor 132
 0.0636
P3358 positive prognostic predictor 70
 0.0337
P3357 negative diagnostic predictor 9
 0.0043
P1057 chromosome 1,426
 0.0023
P6861 dbSNP ID 3
 0.0014
P644 genomic start 1,427
 0.0014
P645 genomic end 1,427
 0.0014
P1929 ClinVar Variation ID 2
 0.0010
P1199 mode of inheritance 1
 0.0005
P10376 ScienceDirect topic ID 1
 0.0003
P1542 has effect 1
 0.0002
P1449 nickname 2
 0.0001
P279 subclass of 87
 0.0000
P10283 OpenAlex ID 3
 0.0000
P31 instance of 1,766
 0.0000
P6366 Microsoft Academic ID 3
 0.0000
P1269 facet of 1
 0.0000
P703 found in taxon 20
 0.0000
P704 Ensembl transcript ID 1
 0.0000
P1050 medical condition 1
 0.0000
P1889 different from 1
 0.0000
P1343 described by source 1
 0.0000
P2671 Google Knowledge Graph ID 7
 0.0000
P18 image 2
 0.0000
P361 part of 1
 0.0000
P646 Freebase ID 1
 0.0000