Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1032129
rs1032129
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0004364
Disease:
Autoimmune Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1032129
rs1032129
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C4310768
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1032129
rs1032129
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C4014795
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1032129
rs1032129
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0020676
Disease:
Hypothyroidism 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1032129
rs1032129
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C3150797
Disease:
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11573824
rs11573824
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0201850
Disease:
Alkaline phosphatase measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs7010267
rs7010267
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0005938
Disease:
Bone Density 		A 0.700 GeneticVariation GWASCAT Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. 29304378 2018
dbSNP: rs7834745
rs7834745
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0200638
Disease:
Eosinophil count procedure 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs7834745
rs7834745
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0200641
Disease:
Blood basophil count (lab test) 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs11573829
rs11573829
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0005938
Disease:
Bone Density 		0.700 GeneticVariation GWASDB Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. 19801982 2009
dbSNP: rs11573885
rs11573885
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0005938
Disease:
Bone Density 		0.700 GeneticVariation GWASDB Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. 19801982 2009
dbSNP: rs1485289
rs1485289
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0005938
Disease:
Bone Density 		0.700 GeneticVariation GWASDB Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. 19801982 2009
dbSNP: rs1905786
rs1905786
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0005938
Disease:
Bone Density 		0.700 GeneticVariation GWASDB Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. 19801982 2009
dbSNP: rs2073617
rs2073617
Entrez Id: 4982;10584
Gene Symbol: TNFRSF11B;COLEC10
TNFRSF11B;COLEC10
CUI: C0005938
Disease:
Bone Density 		0.700 GeneticVariation GWASDB Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. 19801982 2009
dbSNP: rs2073618
rs2073618
Entrez Id: 4982;10584
Gene Symbol: TNFRSF11B;COLEC10
TNFRSF11B;COLEC10
CUI: C0005938
Disease:
Bone Density 		0.700 GeneticVariation GWASDB Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. 19801982 2009
dbSNP: rs3134063
rs3134063
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0005938
Disease:
Bone Density 		0.700 GeneticVariation GWASDB Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. 19801982 2009
dbSNP: rs4319131
rs4319131
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0005938
Disease:
Bone Density 		0.700 GeneticVariation GWASDB Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. 19801982 2009
dbSNP: rs6415470
rs6415470
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0005938
Disease:
Bone Density 		0.700 GeneticVariation GWASDB Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. 19801982 2009
dbSNP: rs6469788
rs6469788
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0005938
Disease:
Bone Density 		0.700 GeneticVariation GWASDB Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. 19801982 2009
dbSNP: rs6469789
rs6469789
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0005938
Disease:
Bone Density 		0.700 GeneticVariation GWASDB Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. 19801982 2009
dbSNP: rs7463176
rs7463176
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0005938
Disease:
Bone Density 		0.700 GeneticVariation GWASDB Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. 19801982 2009
dbSNP: rs7464496
rs7464496
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0005938
Disease:
Bone Density 		0.700 GeneticVariation GWASDB Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. 19801982 2009
dbSNP: rs104894091
rs104894091
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0268414
Disease:
Hyperphosphatasemia with bone disease 		T 0.700 CausalMutation CLINVAR
dbSNP: rs104894092
rs104894092
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0268414
Disease:
Hyperphosphatasemia with bone disease 		G 0.700 CausalMutation CLINVAR
dbSNP: rs200071478
rs200071478
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
CUI: C0268414
Disease:
Hyperphosphatasemia with bone disease 		G 0.700 CausalMutation CLINVAR