Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10489261
rs10489261
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs114017545
rs114017545
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12564992
rs12564992
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs61828641
rs61828641
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs61828641
rs61828641
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs79589199
rs79589199
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs79589199
rs79589199
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs333418
rs333418
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs6666767
rs6666767
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
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: rs7512930
rs7512930
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs75650221
rs75650221
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C0525045
Disease:
Mood Disorders 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs75650221
rs75650221
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C1269683
Disease:
Major Depressive Disorder 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs913687
rs913687
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C0525045
Disease:
Mood Disorders 		0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs913687
rs913687
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C1269683
Disease:
Major Depressive Disorder 		0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs17301853
rs17301853
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C0338480
Disease:
Common Migraine 		0.700 GeneticVariation GWASDB Genome-wide meta-analysis identifies new susceptibility loci for migraine. 23793025 2013
dbSNP: rs17301853
rs17301853
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C0149931
Disease:
Migraine Disorders 		0.700 GeneticVariation GWASCAT Genome-wide meta-analysis identifies new susceptibility loci for migraine. 23793025 2013
dbSNP: rs1890881
rs1890881
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C0001973
Disease:
Alcoholic Intoxication, Chronic 		0.010 GeneticVariation BEFREE One GWS region (chromosome 1: rs1890881) emerged from a trans-ancestral meta-analysis (EA + AA) of ANYDEP, and was attributable to alcohol dependence in both samples. 31099175 2019
dbSNP: rs61826952
rs61826952
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C0001973
Disease:
Alcoholic Intoxication, Chronic 		0.010 GeneticVariation BEFREE In the trans-ancestral meta-analysis, rs1229984 was associated with multiple phenotypes and two additional loci were genome-wide significant: rs61826952 (chromosome 1, DSM-IV AD, P = 8.42E-11); rs7597960 (chromosome 2, Time spent drinking, P = 1.22E-08). 31090166 2019
dbSNP: rs12078839
rs12078839
Entrez Id: 9910
Gene Symbol: RABGAP1L
RABGAP1L
CUI: C0020538
Disease:
Hypertensive disease 		0.010 GeneticVariation BEFREE The A-->G polymorphism (rs645106) of SDK1 and the C-->G polymorphism (rs12078839) of RABGAP1L were significantly associated with hypertension in subject panel B. Multivariable logistic regression analysis with adjustment for covariates, as well as a stepwise forward selection procedure revealed that the A-->G polymorphism of SDK1 was significantly associated with hypertension in both subject panels A and B, with the G allele protecting against this condition. 19851296 2010