Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs755846060
rs755846060
Entrez Id: 10370
Gene Symbol: CITED2
CITED2
CUI: C0010068
Disease:
Coronary heart disease
0.010 GeneticVariation BEFREE In the present study, 187 unrelated Tibetan patients with CHD and 200 unrelated Tibetan healthy controls were screened for variants in the CITED2 gene; we subsequently identified one potential disease-causing mutation p.G143A in a 6-year-old girl with PDA and functional analyses of the mutation were carried out. 28687891 2017
dbSNP: rs766774041
rs766774041
Entrez Id: 10370
Gene Symbol: CITED2
CITED2
CUI: C1853238
Disease:
Conotruncal defect
0.010 GeneticVariation BEFREE In this study, we screened the coding regions of CITED2 in 605 Chinese children with CTDs and found two possible pathogenic mutant sites: p.Q117L and p.T257A, both located in the conserved regions of CITED2. 28436679 2017
dbSNP: rs146180399
rs146180399
Entrez Id: 10370
Gene Symbol: CITED2
CITED2
CUI: C0085215
Disease:
Ovarian Failure, Premature
0.010 GeneticVariation BEFREE The nonsynonymous variant c.604C>A (p.Pro202Thr) was found uniquely in 1 woman from the POF group. 22709740 2012
dbSNP: rs146180399
rs146180399
Entrez Id: 10370
Gene Symbol: CITED2
CITED2
CUI: C0025322
Disease:
Premature Menopause
0.010 GeneticVariation BEFREE The nonsynonymous variant c.604C>A (p.Pro202Thr) was found uniquely in 1 woman from the POF group. 22709740 2012
dbSNP: rs546772104
rs546772104
Entrez Id: 10370
Gene Symbol: CITED2
CITED2
CUI: C0152021
Disease:
Congenital heart disease
0.010 GeneticVariation BEFREE By screening 1126 sporadic congenital heart disease (CHD) cases and 1227 controls, we identified 19 variants, including 5 unique non-synonymous sequence variations (N62S, R92G, T166N, G180-A187del and A187T) in patients. 23082118 2012
dbSNP: rs563655306
rs563655306
Entrez Id: 10370
Gene Symbol: CITED2
CITED2
CUI: C0003507
Disease:
Aortic Valve Stenosis
0.010 GeneticVariation BEFREE We investigated the function and mechanism of two missense mutations, G184S and S192G, responsible for tetralogy of Fallot and aortic stenosis, respectively. 22735262 2012
dbSNP: rs563655306
rs563655306
Entrez Id: 10370
Gene Symbol: CITED2
CITED2
CUI: C0039685
Disease:
Tetralogy of Fallot
0.010 GeneticVariation BEFREE We investigated the function and mechanism of two missense mutations, G184S and S192G, responsible for tetralogy of Fallot and aortic stenosis, respectively. 22735262 2012