RXRG, retinoid X receptor gamma, 6258

N. diseases: 40; N. variants: 9
Disease: Age at menarche ×
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: 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