Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10083447
rs10083447
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1133441
rs1133441
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs149079426
rs149079426
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C2745953
Disease:
Spondylometaphyseal dysplasia with dentinogenesis imperfecta 		A 0.700 CausalMutation CLINVAR Hypomorphic mutations of TRIP11 cause odontochondrodysplasia. 30728324 2019
dbSNP: rs1566843321
rs1566843321
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C2745953
Disease:
Spondylometaphyseal dysplasia with dentinogenesis imperfecta 		C 0.700 GeneticVariation CLINVAR Hypomorphic mutations of TRIP11 cause odontochondrodysplasia. 30728324 2019
dbSNP: rs1566863801
rs1566863801
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C2745953
Disease:
Spondylometaphyseal dysplasia with dentinogenesis imperfecta 		A 0.700 GeneticVariation CLINVAR Hypomorphic mutations of TRIP11 cause odontochondrodysplasia. 30728324 2019
dbSNP: rs267607138
rs267607138
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C2745953
Disease:
Spondylometaphyseal dysplasia with dentinogenesis imperfecta 		A 0.700 CausalMutation CLINVAR Hypomorphic mutations of TRIP11 cause odontochondrodysplasia. 30728324 2019
dbSNP: rs780625551
rs780625551
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C2745953
Disease:
Spondylometaphyseal dysplasia with dentinogenesis imperfecta 		A 0.700 GeneticVariation CLINVAR Hypomorphic mutations of TRIP11 cause odontochondrodysplasia. 30728324 2019
dbSNP: rs8007661
rs8007661
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C4049938
Disease:
Physical Activity Measurement 		C 0.700 GeneticVariation GWASCAT Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. 28448500 2017
dbSNP: rs7155279
rs7155279
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0042834
Disease:
Vital capacity 		G 0.700 GeneticVariation GWASCAT Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation. 26635082 2015
dbSNP: rs7155279
rs7155279
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0016529
Disease:
Forced expiratory volume function 		G 0.700 GeneticVariation GWASCAT Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation. 26635082 2015
dbSNP: rs7158300
rs7158300
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0005890
Disease:
Body Height 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci. 25429064 2015
dbSNP: rs1085307101
rs1085307101
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0265273
Disease:
Achondrogenesis type 1A 		A 0.700 GeneticVariation CLINVAR Lethal skeletal dysplasia in mice and humans lacking the golgin GMAP-210. 20089971 2010
dbSNP: rs7155279
rs7155279
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0005890
Disease:
Body Height 		T 0.700 GeneticVariation GWASCAT Hundreds of variants clustered in genomic loci and biological pathways affect human height. 20881960 2010
dbSNP: rs7155279
rs7155279
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0489786
Disease:
Height 		T 0.700 GeneticVariation GWASDB Hundreds of variants clustered in genomic loci and biological pathways affect human height. 20881960 2010
dbSNP: rs8007661
rs8007661
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0489786
Disease:
Height 		T 0.700 GeneticVariation GWASDB Identification of ten loci associated with height highlights new biological pathways in human growth. 18391950 2008
dbSNP: rs8007661
rs8007661
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0005890
Disease:
Body Height 		T 0.700 GeneticVariation GWASCAT Identification of ten loci associated with height highlights new biological pathways in human growth. 18391950 2008
dbSNP: rs1053206465
rs1053206465
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0265273
Disease:
Achondrogenesis type 1A 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1294029121
rs1294029121
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0265273
Disease:
Achondrogenesis type 1A 		T 0.700 CausalMutation CLINVAR
dbSNP: rs139539448
rs139539448
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0265273
Disease:
Achondrogenesis type 1A 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0349588
Disease:
Short stature 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0085207
Disease:
Gestational Diabetes 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C1863008
Disease:
Yellow-brown discoloration of the teeth 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0878659
Disease:
Disproportionate short stature 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C4021739
Disease:
Abnormality of the acetabulum 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C1865017
Disease:
Thin upper lip vermilion 		A 0.700 CausalMutation CLINVAR