Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12481546
rs12481546
AAR2
CUI: C0005890
Disease: Body Height
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs17436024
rs17436024
AAR2
CUI: C1168438
Disease: Protein C antigen measurement
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
AAR2
CUI: C0919677
Disease: Protein C measurement
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: rs2425192
rs2425192
AAR2
CUI: C0406208
Disease: Suntan
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: rs2425204
rs2425204
AAR2
CUI: C1168438
Disease: Protein C antigen measurement
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
AAR2
CUI: C0919677
Disease: Protein C measurement
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
AAR2
CUI: C1838705
Disease: Anteriorly placed anus
Anteriorly placed anus 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs746800707
rs746800707
AAR2
CUI: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs746800707
rs746800707
AAR2
CUI: C0332573
Disease: Macule
Macule 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs746800707
rs746800707
AAR2
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs746800707
rs746800707
AAR2
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs746800707
rs746800707
AAR2
CUI: C4025708
Disease: Cerebellar malformation
Cerebellar malformation 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs746800707
rs746800707
AAR2
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding) 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs746800707
rs746800707
AAR2
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		A 0.700 GeneticVariation CLINVAR