TTC19, tetratricopeptide repeat domain 19, 54902

N. diseases: 78; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1075901
rs1075901
Entrez Id: 9611;54902
Gene Symbol: NCOR1;TTC19
NCOR1;TTC19
CUI: C1305855
Disease:
Body mass index 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs1075901
rs1075901
Entrez Id: 9611;54902
Gene Symbol: NCOR1;TTC19
NCOR1;TTC19
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1187416161
rs1187416161
Entrez Id: 54902
Gene Symbol: TTC19
TTC19
CUI: C3554605
Disease:
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1555530551
rs1555530551
Entrez Id: 54902
Gene Symbol: TTC19
TTC19
CUI: C3554605
Disease:
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 		T 0.700 CausalMutation CLINVAR
dbSNP: rs387907094
rs387907094
Entrez Id: 54902
Gene Symbol: TTC19
TTC19
CUI: C3554605
Disease:
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 		T 0.700 CausalMutation CLINVAR
dbSNP: rs747166010
rs747166010
Entrez Id: 54902
Gene Symbol: TTC19
TTC19
CUI: C3554605
Disease:
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 		G 0.700 CausalMutation CLINVAR
dbSNP: rs794726691
rs794726691
Entrez Id: 54902
Gene Symbol: TTC19
TTC19
CUI: C3554605
Disease:
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 		T 0.700 CausalMutation CLINVAR
dbSNP: rs794726692
rs794726692
Entrez Id: 54902
Gene Symbol: TTC19
TTC19
CUI: C3554605
Disease:
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 		T 0.700 CausalMutation CLINVAR