Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: C1868684
Disease:
EAR, PATELLA, SHORT STATURE SYNDROME
A 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
dbSNP: rs864309488
rs864309488
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C1868684
Disease:
EAR, PATELLA, SHORT STATURE SYNDROME
G 0.700 GeneticVariation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015