As of 2022-03-07, the Wikidata property dbSNP ID (P6861) is used on 18 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
P31 instance of 18
 0.0000
P1057 chromosome 12
 0.0000
P644 genomic start 9
 0.0000
P645 genomic end 9
 0.0000
P6366 Microsoft Academic ID 6
 0.0000
P646 Freebase ID 6
 0.0000
P3331 HGVS nomenclature 5
 0.0053
P1929 ClinVar Variation ID 3
 0.1667
P3433 biological variant of 3
 0.0014
P1269 facet of 3
 0.0000
P10283 OpenAlex ID 3
 0.0000
P361 part of 3
 0.0000
P3355 negative therapeutic predictor 2
 0.0041
P3329 CIViC variant ID 2
 0.0010
P1542 has effect 2
 0.0005
P1199 mode of inheritance 1
 0.0099
P3356 positive diagnostic predictor 1
 0.0067
P3359 negative prognostic predictor 1
 0.0047
P3354 positive therapeutic predictor 1
 0.0017
P2293 genetic association 1
 0.0001
P704 Ensembl transcript ID 1
 0.0000
P1050 medical condition 1
 0.0000
P1889 different from 1
 0.0000
P973 described at URL 1
 0.0000
P1343 described by source 1
 0.0000
P688 encodes 1
 0.0000
P856 official website 1
 0.0000
P703 found in taxon 1
 0.0000
P279 subclass of 1
 0.0000
P373 Commons category 1
 0.0000
P2671 Google Knowledge Graph ID 1
 0.0000

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P1929 ClinVar Variation ID 3
 0.1667
P1199 mode of inheritance 1
 0.0099
P3356 positive diagnostic predictor 1
 0.0067
P3331 HGVS nomenclature 5
 0.0053
P3359 negative prognostic predictor 1
 0.0047
P3355 negative therapeutic predictor 2
 0.0041
P3354 positive therapeutic predictor 1
 0.0017
P3433 biological variant of 3
 0.0014
P3329 CIViC variant ID 2
 0.0010
P1542 has effect 2
 0.0005
P2293 genetic association 1
 0.0001
P1269 facet of 3
 0.0000
P10283 OpenAlex ID 3
 0.0000
P6366 Microsoft Academic ID 6
 0.0000
P1057 chromosome 12
 0.0000
P644 genomic start 9
 0.0000
P645 genomic end 9
 0.0000
P704 Ensembl transcript ID 1
 0.0000
P1050 medical condition 1
 0.0000
P1889 different from 1
 0.0000
P973 described at URL 1
 0.0000
P1343 described by source 1
 0.0000
P646 Freebase ID 6
 0.0000
P688 encodes 1
 0.0000
P361 part of 3
 0.0000
P856 official website 1
 0.0000
P703 found in taxon 1
 0.0000
P279 subclass of 1
 0.0000
P373 Commons category 1
 0.0000
P31 instance of 18
 0.0000
P2671 Google Knowledge Graph ID 1
 0.0000