TRNQ, tRNA, 4572

N. diseases: 137; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199476140
rs199476140
Entrez Id: 4512;4535;4536;4572
Gene Symbol: COX1;ND1;ND2;TRNQ
COX1;ND1;ND2;TRNQ
CUI: C0026848
Disease:
Myopathy 		CA 0.700 CausalMutation CLINVAR
dbSNP: rs199476141
rs199476141
Entrez Id: 4512;4535;4536;4572
Gene Symbol: COX1;ND1;ND2;TRNQ
COX1;ND1;ND2;TRNQ
CUI: C0162671
Disease:
MELAS Syndrome 		A 0.700 CausalMutation CLINVAR
dbSNP: rs41456348
rs41456348
Entrez Id: 4512;4535;4536;4572
Gene Symbol: COX1;ND1;ND2;TRNQ
COX1;ND1;ND2;TRNQ
CUI: C4016609
Disease:
SENSORINEURAL DEAFNESS AND MIGRAINE 		C 0.700 CausalMutation CLINVAR