As of 2022-03-07, the Wikidata property HGVS nomenclature (P3331) is used on 928 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
P3433 biological variant of 926
 0.4454
P1057 chromosome 926
 0.0015
P644 genomic start 926
 0.0009
P645 genomic end 926
 0.0009
P31 instance of 925
 0.0000
P3329 CIViC variant ID 837
 0.4075
P3355 negative therapeutic predictor 283
 0.2547
P3354 positive therapeutic predictor 233
 0.1843
P279 subclass of 87
 0.0000
P3359 negative prognostic predictor 44
 0.0407
P3356 positive diagnostic predictor 30
 0.0291
P3358 positive prognostic predictor 16
 0.0163
P6861 dbSNP ID 5
 0.0053
P1929 ClinVar Variation ID 3
 0.0032
P3357 negative diagnostic predictor 3
 0.0032
P10283 OpenAlex ID 2
 0.0000
P6366 Microsoft Academic ID 2
 0.0000
P361 part of 2
 0.0000
P2671 Google Knowledge Graph ID 2
 0.0000
P1199 mode of inheritance 1
 0.0010
P1542 has effect 1
 0.0002
P2293 genetic association 1
 0.0001
P704 Ensembl transcript ID 1
 0.0000
P1050 medical condition 1
 0.0000
P1343 described by source 1
 0.0000
P688 encodes 1
 0.0000
P856 official website 1
 0.0000
P646 Freebase ID 1
 0.0000

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P3433 biological variant of 926
 0.4454
P3329 CIViC variant ID 837
 0.4075
P3355 negative therapeutic predictor 283
 0.2547
P3354 positive therapeutic predictor 233
 0.1843
P3359 negative prognostic predictor 44
 0.0407
P3356 positive diagnostic predictor 30
 0.0291
P3358 positive prognostic predictor 16
 0.0163
P6861 dbSNP ID 5
 0.0053
P1929 ClinVar Variation ID 3
 0.0032
P3357 negative diagnostic predictor 3
 0.0032
P1057 chromosome 926
 0.0015
P1199 mode of inheritance 1
 0.0010
P644 genomic start 926
 0.0009
P645 genomic end 926
 0.0009
P1542 has effect 1
 0.0002
P2293 genetic association 1
 0.0001
P279 subclass of 87
 0.0000
P10283 OpenAlex ID 2
 0.0000
P31 instance of 925
 0.0000
P6366 Microsoft Academic ID 2
 0.0000
P704 Ensembl transcript ID 1
 0.0000
P1050 medical condition 1
 0.0000
P1343 described by source 1
 0.0000
P688 encodes 1
 0.0000
P361 part of 2
 0.0000
P856 official website 1
 0.0000
P2671 Google Knowledge Graph ID 2
 0.0000
P646 Freebase ID 1
 0.0000