HMG20B, high mobility group 20B, 10362

N. diseases: 8; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs56208656
rs56208656
Entrez Id: 10362
Gene Symbol: HMG20B
HMG20B
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1014264982
rs1014264982
Entrez Id: 10362
Gene Symbol: HMG20B
HMG20B
CUI: C0242379
Disease:
Malignant neoplasm of lung 		0.010 GeneticVariation BEFREE The non-conservative substitution of HMG20b residue Ala247 with Pro, reported in human lung cancer, disrupts these activities of HMG20b, impairing cytokinesis in a trans-dominant manner. 25486196 2014
dbSNP: rs1014264982
rs1014264982
Entrez Id: 10362
Gene Symbol: HMG20B
HMG20B
CUI: C1306460
Disease:
Primary malignant neoplasm of lung 		0.010 GeneticVariation BEFREE The non-conservative substitution of HMG20b residue Ala247 with Pro, reported in human lung cancer, disrupts these activities of HMG20b, impairing cytokinesis in a trans-dominant manner. 25486196 2014
dbSNP: rs1014264982
rs1014264982
Entrez Id: 10362
Gene Symbol: HMG20B
HMG20B
CUI: C0684249
Disease:
Carcinoma of lung 		0.010 GeneticVariation BEFREE The non-conservative substitution of HMG20b residue Ala247 with Pro, reported in human lung cancer, disrupts these activities of HMG20b, impairing cytokinesis in a trans-dominant manner. 25486196 2014