Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs863223281
rs863223281
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0265273
Disease:
Achondrogenesis type 1A 		C 0.700 CausalMutation CLINVAR
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: 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: 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: rs780625551
rs780625551
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0029422
Disease:
Osteochondrodysplasias 		A 0.700 CausalMutation CLINVAR
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: 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: 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: 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: 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: rs34761938
rs34761938
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0265273
Disease:
Achondrogenesis type 1A 		T 0.700 CausalMutation CLINVAR
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: rs267607138
rs267607138
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0265273
Disease:
Achondrogenesis type 1A 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1566867763
rs1566867763
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0265273
Disease:
Achondrogenesis type 1A 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1566863801
rs1566863801
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0029422
Disease:
Osteochondrodysplasias 		A 0.700 CausalMutation CLINVAR
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: rs1566860640
rs1566860640
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0265273
Disease:
Achondrogenesis type 1A 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1566860640
rs1566860640
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0029422
Disease:
Osteochondrodysplasias 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1566859649
rs1566859649
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0029422
Disease:
Osteochondrodysplasias 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1566859264
rs1566859264
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0265273
Disease:
Achondrogenesis type 1A 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1566843321
rs1566843321
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0029422
Disease:
Osteochondrodysplasias 		C 0.700 CausalMutation CLINVAR
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: rs1555386022
rs1555386022
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C4072904
Disease:
Secondary Caesarian section 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1555386022
rs1555386022
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C4281993
Disease:
Neonatal respiratory distress 		A 0.700 CausalMutation CLINVAR