Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13282289
rs13282289
Entrez Id: 51435
Gene Symbol: SCARA3
SCARA3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs34951274
rs34951274
Entrez Id: 51435
Gene Symbol: SCARA3
SCARA3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies. 31564439 2019
dbSNP: rs557942
rs557942
Entrez Id: 51435
Gene Symbol: SCARA3
SCARA3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs485902
rs485902
Entrez Id: 51435
Gene Symbol: SCARA3
SCARA3
CUI: C0002395
Disease:
Alzheimer's Disease 		0.700 GeneticVariation GWASCAT GWAS on family history of Alzheimer's disease. 29777097 2018
dbSNP: rs519238
rs519238
Entrez Id: 51435
Gene Symbol: SCARA3
SCARA3
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs519238
rs519238
Entrez Id: 51435
Gene Symbol: SCARA3
SCARA3
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018