GMNN, geminin DNA replication inhibitor, 51053

N. diseases: 153; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs864309488
rs864309488
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C4225188
Disease:
MEIER-GORLIN SYNDROME 6 		0.800 GeneticVariation UNIPROT
dbSNP: rs864309488
rs864309488
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C4225188
Disease:
MEIER-GORLIN SYNDROME 6 		G 0.800 CausalMutation CLINVAR
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C4225188
Disease:
MEIER-GORLIN SYNDROME 6 		T 0.700 CausalMutation CLINVAR
dbSNP: rs864309487
rs864309487
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C4225188
Disease:
MEIER-GORLIN SYNDROME 6 		A 0.700 CausalMutation CLINVAR
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C0152423
Disease:
Congenital small ears 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C1866190
Disease:
Atresia of the external auditory canal 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C0025990
Disease:
Micrognathism 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C1386048
Disease:
Intrauterine retardation 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C0541764
Disease:
Delayed bone age 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C0014390
Disease:
Entropion 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C4022715
Disease:
Hypoplastic female external genitalia 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C0019322
Disease:
Umbilical hernia 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C1836543
Disease:
Thick vermilion border 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C0238441
Disease:
Subglottic stenosis 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C0948187
Disease:
Tracheomalacia 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C1837260
Disease:
Prominent forehead 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C4023343
Disease:
Nasogastric tube feeding in infancy 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C1855514
Disease:
Severe failure to thrive 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C1868578
Disease:
Patellar aplasia 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C4025406
Disease:
Abnormality of the middle phalanx of the 5th finger 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C1857641
Disease:
Severe postnatal growth retardation 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C0423110
Disease:
Downward slant of palpebral fissure 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C1840077
Disease:
Anteverted nostril 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309486
rs864309486
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C1868684
Disease:
EAR, PATELLA, SHORT STATURE SYNDROME 		T 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309487
rs864309487
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C0423112
Disease:
Short palpebral fissure 		A 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015