RXRG, retinoid X receptor gamma, 6258

N. diseases: 40; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs466639
rs466639
Entrez Id: 6258
Gene Symbol: RXRG
RXRG
CUI: C1314691
Disease:
Age at menarche
C 0.800 GeneticVariation GWASCAT Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. 25231870 2014
dbSNP: rs285480
rs285480
Entrez Id: 6258
Gene Symbol: RXRG
RXRG
CUI: C0233849
Disease:
Personality Traits
0.800 GeneticVariation GWASCAT Genome-wide association study of personality traits in bipolar patients. 21368711 2011
dbSNP: rs285480
rs285480
Entrez Id: 6258
Gene Symbol: RXRG
RXRG
CUI: C0233849
Disease:
Personality Traits
0.800 GeneticVariation GWASDB Genome-wide association study of personality traits in bipolar patients. 21368711 2011
dbSNP: rs466639
rs466639
Entrez Id: 6258
Gene Symbol: RXRG
RXRG
CUI: C1314691
Disease:
Age at menarche
T 0.800 GeneticVariation GWASCAT Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. 21102462 2010
dbSNP: rs466639
rs466639
Entrez Id: 6258
Gene Symbol: RXRG
RXRG
CUI: C1314691
Disease:
Age at menarche
T 0.800 GeneticVariation GWASDB Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. 21102462 2010
dbSNP: rs2194899
rs2194899
Entrez Id: 6258
Gene Symbol: RXRG
RXRG
CUI: C1314691
Disease:
Age at menarche
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10489744
rs10489744
Entrez Id: 6258
Gene Symbol: RXRG
RXRG
CUI: C0005586
Disease:
Bipolar Disorder
0.700 GeneticVariation GWASCAT Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis. 27890468 2017
dbSNP: rs10489744
rs10489744
Entrez Id: 6258
Gene Symbol: RXRG
RXRG
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder
0.700 GeneticVariation GWASCAT Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis. 27890468 2017
dbSNP: rs100537
rs100537
Entrez Id: 6258
Gene Symbol: RXRG
RXRG
CUI: C1314691
Disease:
Age at menarche
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs17429130
rs17429130
Entrez Id: 6258
Gene Symbol: RXRG
RXRG
CUI: C0085207
Disease:
Gestational Diabetes
0.010 GeneticVariation BEFREE Together, these findings indicate that GC rs16847024, RXRG rs17429130 and RXRA rs4917356 were candidate susceptibility markers for GDM in Chinese females. 27636996 2016
dbSNP: rs3818569
rs3818569
Entrez Id: 6258
Gene Symbol: RXRG
RXRG
CUI: C0524620
Disease:
Metabolic Syndrome X
0.010 GeneticVariation BEFREE For the SNP genotypes of rs362551 (SNAP25), rs3818569 (RXRG), rs1479355, rs1570070 (IGF2R), and rs916829 (ABCC8), heterozygotes showed a lower risk of MetS compared with the reference group. 25867398 2015
dbSNP: rs113471
rs113471
Entrez Id: 6258
Gene Symbol: RXRG
RXRG
CUI: C1708272
Disease:
HIV lipodystrophy
0.010 GeneticVariation BEFREE Three single nucleotide polymorphisms in RXRγ (rs2134095, rs113471, rs2194899) and its haplotypes (HIVLD+, 54%; HIVLD-, 40.6%; P=0.02) showed significant association with HIVLD. 23759678 2013
dbSNP: rs2134095
rs2134095
Entrez Id: 6258
Gene Symbol: RXRG
RXRG
CUI: C1708272
Disease:
HIV lipodystrophy
0.010 GeneticVariation BEFREE Three single nucleotide polymorphisms in RXRγ (rs2134095, rs113471, rs2194899) and its haplotypes (HIVLD+, 54%; HIVLD-, 40.6%; P=0.02) showed significant association with HIVLD. 23759678 2013
dbSNP: rs2194899
rs2194899
Entrez Id: 6258
Gene Symbol: RXRG
RXRG
CUI: C1708272
Disease:
HIV lipodystrophy
0.010 GeneticVariation BEFREE Three single nucleotide polymorphisms in RXRγ (rs2134095, rs113471, rs2194899) and its haplotypes (HIVLD+, 54%; HIVLD-, 40.6%; P=0.02) showed significant association with HIVLD. 23759678 2013
dbSNP: rs3818569
rs3818569
Entrez Id: 6258
Gene Symbol: RXRG
RXRG
CUI: C0011884
Disease:
Diabetic Retinopathy
0.010 GeneticVariation BEFREE One SNP--rs3818569 of the RXR-gamma gene was found to be associated with increased risk for diabetic retinopathy in both allele and genotype frequencies (P = 0.0023 and 0.0057, respectively). 22180072 2011