AAR2, AAR2 splicing factor, 25980

N. diseases: 13; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12481546
rs12481546
Entrez Id: 25980
Gene Symbol: AAR2
AAR2
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2425192
rs2425192
Entrez Id: 25980
Gene Symbol: AAR2
AAR2
CUI: C0406208
Disease:
Suntan 		A 0.700 GeneticVariation GWASCAT Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure. 29739929 2018
dbSNP: rs17436024
rs17436024
Entrez Id: 25980
Gene Symbol: AAR2
AAR2
CUI: C1168438
Disease:
Protein C antigen measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs17436024
rs17436024
Entrez Id: 25980
Gene Symbol: AAR2
AAR2
CUI: C0919677
Disease:
Protein C measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs2425204
rs2425204
Entrez Id: 25980
Gene Symbol: AAR2
AAR2
CUI: C1168438
Disease:
Protein C antigen measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs2425204
rs2425204
Entrez Id: 25980
Gene Symbol: AAR2
AAR2
CUI: C0919677
Disease:
Protein C measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs746800707
rs746800707
Entrez Id: 25980
Gene Symbol: AAR2
AAR2
CUI: C1838705
Disease:
Anteriorly placed anus 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs746800707
rs746800707
Entrez Id: 25980
Gene Symbol: AAR2
AAR2
CUI: C0016522
Disease:
Foramen Ovale, Patent 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs746800707
rs746800707
Entrez Id: 25980
Gene Symbol: AAR2
AAR2
CUI: C0332573
Disease:
Macule 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs746800707
rs746800707
Entrez Id: 25980
Gene Symbol: AAR2
AAR2
CUI: C0344482
Disease:
Hypoplasia of corpus callosum 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs746800707
rs746800707
Entrez Id: 25980
Gene Symbol: AAR2
AAR2
CUI: C0557874
Disease:
Global developmental delay 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs746800707
rs746800707
Entrez Id: 25980
Gene Symbol: AAR2
AAR2
CUI: C4025708
Disease:
Cerebellar malformation 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs746800707
rs746800707
Entrez Id: 25980
Gene Symbol: AAR2
AAR2
CUI: C4551563
Disease:
Microcephaly (physical finding) 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs746800707
rs746800707
Entrez Id: 25980
Gene Symbol: AAR2
AAR2
CUI: C0018818
Disease:
Ventricular Septal Defects 		A 0.700 GeneticVariation CLINVAR