RABGAP1, RAB GTPase activating protein 1, 23637

N. diseases: 5; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10985827
rs10985827
Entrez Id: 23637
Gene Symbol: RABGAP1
RABGAP1
CUI: C0005612
Disease:
Birth Weight 		G 0.700 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758 2019
dbSNP: rs6478585
rs6478585
Entrez Id: 23637
Gene Symbol: RABGAP1
RABGAP1
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs803733
rs803733
Entrez Id: 23637
Gene Symbol: RABGAP1
RABGAP1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs187416346
rs187416346
Entrez Id: 23637
Gene Symbol: RABGAP1
RABGAP1
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs187416346
rs187416346
Entrez Id: 23637
Gene Symbol: RABGAP1
RABGAP1
CUI: C0596887
Disease:
mathematical ability 		G 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs10818775
rs10818775
Entrez Id: 23637
Gene Symbol: RABGAP1
RABGAP1
CUI: C0871470
Disease:
Systolic Pressure 		C 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs700059
rs700059
Entrez Id: 23637
Gene Symbol: RABGAP1
RABGAP1
CUI: C0005612
Disease:
Birth Weight 		G 0.700 GeneticVariation GWASCAT Genome-wide associations for birth weight and correlations with adult disease. 27680694 2016