Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0549306
Disease:
Mesomelia
A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0158986
Disease:
Neonatal hypoglycemia
A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C1096086
Disease:
Deformity of lower limb
A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0454644
Disease:
Delayed speech and language development
A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C1837406
Disease:
Hypoplasia involving bones of the upper limbs
A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C1837658
Disease:
Gross motor development delay
A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0549629
Disease:
Abnormal delivery
A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C1842153
Disease:
Irregular vertebral endplates
A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C4281993
Disease:
Neonatal respiratory distress
A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C4020900
Disease:
Abnormality of the upper limb
A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0024003
Disease:
Lordosis
A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0345371
Disease:
Hypoplasia of lower limb
A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C2745953
Disease:
Spondylometaphyseal dysplasia with dentinogenesis imperfecta
A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C1837482
Disease:
Thoracic hypoplasia
A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0016506
Disease:
Foot Deformities
A 0.700 CausalMutation CLINVAR
dbSNP: rs1400419650
rs1400419650
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0265294
Disease:
Pyle metaphyseal dysplasia
A 0.700 CausalMutation CLINVAR