CDIP1, cell death inducing p53 target 1, 29965

N. diseases: 3; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1051308
rs1051308
Entrez Id: 3163;29965
Gene Symbol: HMOX2;CDIP1
HMOX2;CDIP1
CUI: C0270736
Disease:
Essential Tremor 		0.020 GeneticVariation BEFREE These results suggest that the ALAD rs1800435 SNP is not related with the risk for ET, but its interaction with the HMOX2 rs1051308 SNP could be weakly associated with the risk for this disease. 28276576 2017
dbSNP: rs1051308
rs1051308
Entrez Id: 3163;29965
Gene Symbol: HMOX2;CDIP1
HMOX2;CDIP1
CUI: C0270736
Disease:
Essential Tremor 		0.020 GeneticVariation BEFREE The present study suggests a weak association between HMOX1 rs2071746 and HMOX2 rs1051308 polymorphisms and the risk to develop ET in the Spanish population. 26091465 2015
dbSNP: rs1051308
rs1051308
Entrez Id: 3163;29965
Gene Symbol: HMOX2;CDIP1
HMOX2;CDIP1
CUI: C0030567
Disease:
Parkinson Disease 		0.010 GeneticVariation BEFREE Our results suggest that rs1051308 is associated with risk of developing PD in Han Chinese, and further studies involving various ethnicities are needed to validate the association. 28179208 2017
dbSNP: rs1051308
rs1051308
Entrez Id: 3163;29965
Gene Symbol: HMOX2;CDIP1
HMOX2;CDIP1
CUI: C0242383
Disease:
Age related macular degeneration 		0.010 GeneticVariation BEFREE In the present work we analyzed the association between the c.544G>A polymorphism of the heme oxygenase-2 gene (HMOX2) (rs1051308) and AMD. 21804464 2011