TRIM8, tripartite motif containing 8, 81603

N. diseases: 43; N. variants: 1
Source: CLINVAR ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C1142533
Disease:
Smooth philtrum 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0034065
Disease:
Pulmonary Embolism 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0578038
Disease:
Thin lips 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0270834
Disease:
Complex partial seizure with impairment of consciousness 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0025990
Disease:
Micrognathism 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0520679
Disease:
Sleep Apnea, Obstructive 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0085207
Disease:
Gestational Diabetes 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0576227
Disease:
Narrow foot 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0232466
Disease:
Feeding difficulties 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0001807
Disease:
Aggressive behavior 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0020676
Disease:
Hypothyroidism 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0018808
Disease:
Heart murmur 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0016202
Disease:
Flatfoot 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0557874
Disease:
Global developmental delay 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0151878
Disease:
Prolonged QT interval 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0038220
Disease:
Status Epilepticus 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0565599
Disease:
Maternal hypertension 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0004106
Disease:
Astigmatism 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0003706
Disease:
Arachnodactyly 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0549629
Disease:
Abnormal delivery 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0036572
Disease:
Seizures 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C1837731
Disease:
Overfolded helix 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0740279
Disease:
Cerebellar atrophy 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C1305740
Disease:
Overbite 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs866294686
rs866294686
Entrez Id: 81603;105378460
Gene Symbol: TRIM8;LOC105378460
TRIM8;LOC105378460
CUI: C0085271
Disease:
Self-Injurious Behavior 		T 0.700 GeneticVariation CLINVAR