RAB27B, RAB27B, member RAS oncogene family, 5874

N. diseases: 64; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12454204
rs12454204
Entrez Id: 5874
Gene Symbol: RAB27B
RAB27B
CUI: C1305855
Disease:
Body mass index 		T 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: rs58243949
rs58243949
Entrez Id: 5874
Gene Symbol: RAB27B
RAB27B
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs62091461
rs62091461
Entrez Id: 5874
Gene Symbol: RAB27B
RAB27B
CUI: C1269683
Disease:
Major Depressive Disorder 		C 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions. 30718901 2019
dbSNP: rs8092503
rs8092503
Entrez Id: 5874
Gene Symbol: RAB27B
RAB27B
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: rs1833288
rs1833288
Entrez Id: 5874
Gene Symbol: RAB27B
RAB27B
CUI: C1269683
Disease:
Major Depressive Disorder 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. 29700475 2018
dbSNP: rs28687557
rs28687557
Entrez Id: 5874
Gene Symbol: RAB27B
RAB27B
CUI: C0525045
Disease:
Mood Disorders 		G 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: rs28687557
rs28687557
Entrez Id: 5874
Gene Symbol: RAB27B
RAB27B
CUI: C1269683
Disease:
Major Depressive Disorder 		G 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: rs8092503
rs8092503
Entrez Id: 5874
Gene Symbol: RAB27B
RAB27B
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT A Large Multiethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci. 30108127 2018
dbSNP: rs7243785
rs7243785
Entrez Id: 5874
Gene Symbol: RAB27B
RAB27B
CUI: C1305855
Disease:
Body mass index 		G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 112 new loci for body mass index in the Japanese population. 28892062 2017
dbSNP: rs8092503
rs8092503
Entrez Id: 5874
Gene Symbol: RAB27B
RAB27B
CUI: C1305855
Disease:
Body mass index 		G 0.700 GeneticVariation GWASCAT Per additional risk allele, body mass index increased 0.04 Standard Deviation Score (SDS) [Standard Error (SE) 0.007], 0.05 SDS (SE 0.008) and 0.14 SDS (SE 0.025), for rs13253111, rs8092503 and rs13387838, respectively. 26604143 2016
dbSNP: rs2311126
rs2311126
Entrez Id: 5874
Gene Symbol: RAB27B
RAB27B
CUI: C0003868
Disease:
Arthritis, Gouty 		0.700 GeneticVariation GWASCAT Genome-wide association study identifies ABCG2 (BCRP) as an allopurinol transporter and a determinant of drug response. 25676789 2015
dbSNP: rs2311126
rs2311126
Entrez Id: 5874
Gene Symbol: RAB27B
RAB27B
CUI: C0018099
Disease:
Gout 		0.700 GeneticVariation GWASCAT Genome-wide association study identifies ABCG2 (BCRP) as an allopurinol transporter and a determinant of drug response. 25676789 2015
dbSNP: rs2311126
rs2311126
Entrez Id: 5874
Gene Symbol: RAB27B
RAB27B
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.700 GeneticVariation GWASCAT Genome-wide association study identifies ABCG2 (BCRP) as an allopurinol transporter and a determinant of drug response. 25676789 2015
dbSNP: rs2311120
rs2311120
Entrez Id: 5874
Gene Symbol: RAB27B
RAB27B
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		0.010 GeneticVariation BEFREE The linkage region on chromosome 18q overlaps with the findings of association of rs2311120 (P=10(-5)) and rs4149601 (P=10(-4)) in the genome-wide association analysis for ADHD performed by the Genetic Association Information Network consortium. 19156173 2009