GNAI3, G protein subunit alpha i3, 2773

N. diseases: 75; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907178
rs387907178
Entrez Id: 2773
Gene Symbol: GNAI3
GNAI3
CUI: C4551996
Disease:
Auriculocondylar syndrome 1 		C 0.800 CausalMutation CLINVAR A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome. 22560091 2012
dbSNP: rs387907178
rs387907178
Entrez Id: 2773
Gene Symbol: GNAI3
GNAI3
CUI: C4551996
Disease:
Auriculocondylar syndrome 1 		0.800 GeneticVariation UNIPROT A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome. 22560091 2012
dbSNP: rs6537837
rs6537837
Entrez Id: 2773
Gene Symbol: GNAI3
GNAI3
CUI: C1269683
Disease:
Major Depressive Disorder 		T 0.800 GeneticVariation GWASCAT Genome-wide association study of recurrent early-onset major depressive disorder. 20125088 2011
dbSNP: rs6537837
rs6537837
Entrez Id: 2773
Gene Symbol: GNAI3
GNAI3
CUI: C1269683
Disease:
Major Depressive Disorder 		T 0.800 GeneticVariation GWASDB Genome-wide association study of recurrent early-onset major depressive disorder. 20125088 2011
dbSNP: rs397514768
rs397514768
Entrez Id: 2773
Gene Symbol: GNAI3
GNAI3
CUI: C4551996
Disease:
Auriculocondylar syndrome 1 		A 0.700 CausalMutation CLINVAR
dbSNP: rs6692804
rs6692804
Entrez Id: 2773
Gene Symbol: GNAI3
GNAI3
CUI: C4511452
Disease:
Sporadic Parkinson disease 		0.010 GeneticVariation BEFREE By single marker analysis, only one marker was significantly associated with PD risk in one of our sample sets (rs6692804: P = 0.03). 18628988 2008