rs11205277, None

N. diseases: 5
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. 30166351 2018
Smoking Behaviors
CUI: C1519383
Disease: Smoking Behaviors
0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. 28443625 2017
Smoking
CUI: C0037369
Disease: Smoking
0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. 28443625 2017
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci. 25429064 2015
Height
CUI: C0489786
Disease: Height
0.700 GeneticVariation GWASDB Hundreds of variants clustered in genomic loci and biological pathways affect human height. 20881960 2010
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT Hundreds of variants clustered in genomic loci and biological pathways affect human height. 20881960 2010
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT Many sequence variants affecting diversity of adult human height. 18391951 2008
Height
CUI: C0489786
Disease: Height
0.700 GeneticVariation GWASDB Many sequence variants affecting diversity of adult human height. 18391951 2008
Nager syndrome
CUI: C0265245
Disease: Nager syndrome
0.010 GeneticVariation BEFREE A significant association with 1st-year height SD score increase during GH treatment was observed with rs11205277, located near 4 known genes: MTMR11, SV2A, HIST2H2AA3, and SF3B4; the latter, in which heterozygous mutations occur in Nager acrofacial dysostosis, appears the most relevant gene. 30970347 2019