RAP1A, RAP1A, member of RAS oncogene family, 5906

N. diseases: 215; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs494453
rs494453
Entrez Id: 5906;643329
Gene Symbol: RAP1A;KRT18P57
RAP1A;KRT18P57
CUI: C0029456
Disease:
Osteoporosis 		C 0.800 GeneticVariation GWASDB An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. 20548944 2010
dbSNP: rs494453
rs494453
Entrez Id: 5906;643329
Gene Symbol: RAP1A;KRT18P57
RAP1A;KRT18P57
CUI: C0029456
Disease:
Osteoporosis 		C 0.800 GeneticVariation GWASCAT An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. 20548944 2010
dbSNP: rs2477432
rs2477432
Entrez Id: 5906
Gene Symbol: RAP1A
RAP1A
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs2477432
rs2477432
Entrez Id: 5906
Gene Symbol: RAP1A
RAP1A
CUI: C0036341
Disease:
Schizophrenia 		0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs2789546
rs2789546
Entrez Id: 5906;100129269
Gene Symbol: RAP1A;LINC01160
RAP1A;LINC01160
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12038204
rs12038204
Entrez Id: 5906;55924
Gene Symbol: RAP1A;INKA2
RAP1A;INKA2
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: rs2477425
rs2477425
Entrez Id: 5906;100129269
Gene Symbol: RAP1A;LINC01160
RAP1A;LINC01160
CUI: C0596887
Disease:
mathematical ability 		T 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: rs9988442
rs9988442
Entrez Id: 5906;57413
Gene Symbol: RAP1A;TMIGD3
RAP1A;TMIGD3
CUI: C0202236
Disease:
Triglycerides measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs6573
rs6573
Entrez Id: 5906;55924
Gene Symbol: RAP1A;INKA2
RAP1A;INKA2
CUI: C0279626
Disease:
Squamous cell carcinoma of esophagus 		0.010 GeneticVariation BEFREE Our study highlights RAP1A and SNP rs6573 functioning as potential personal diagnostic and prognosis markers for ESCC. 22859270 2012