Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C1142533
Disease: Smooth philtrum
Smooth philtrum 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0578038
Disease: Thin lips
Thin lips 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0270834
Disease: Complex partial seizure with impairment of consciousness
Complex partial seizure with impairment of consciousness 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0025990
Disease: Micrognathism
Micrognathism 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0576227
Disease: Narrow foot
Narrow foot 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0018808
Disease: Heart murmur
Heart murmur 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0016202
Disease: Flatfoot
Flatfoot 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0151878
Disease: Prolonged QT interval
Prolonged QT interval 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0038220
Disease: Status Epilepticus
Status Epilepticus 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0565599
Disease: Maternal hypertension
Maternal hypertension 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0004106
Disease: Astigmatism
Astigmatism 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0036572
Disease: Seizures
Seizures 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C1837731
Disease: Overfolded helix
Overfolded helix 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C1305740
Disease: Overbite
Overbite 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
CUI: C0085271
Disease: Self-Injurious Behavior
Self-Injurious Behavior 		T 0.700 GeneticVariation CLINVAR