rs1042725, HMGA2

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Birth Weight
CUI: C0005612
Disease: Birth Weight
0.800 GeneticVariation GWASDB New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism. 23202124 2013
Birth Weight
CUI: C0005612
Disease: Birth Weight
0.800 GeneticVariation GWASCAT New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism. 23202124 2013
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
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
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT Identification of ten loci associated with height highlights new biological pathways in human growth. 18391950 2008
Height
CUI: C0489786
Disease: Height
0.700 GeneticVariation GWASDB Identification of ten loci associated with height highlights new biological pathways in human growth. 18391950 2008
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT Genome-wide association analysis identifies 20 loci that influence adult height. 18391952 2008
Height
CUI: C0489786
Disease: Height
0.700 GeneticVariation GWASDB Genome-wide association analysis identifies 20 loci that influence adult height. 18391952 2008
Height
CUI: C0489786
Disease: Height
0.700 GeneticVariation GWASDB We estimate that rs1042725 explains approximately 0.3% of population variation in height (approximately 0.4 cm increased adult height per C allele). 17767157 2007
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT A common variant of HMGA2 is associated with adult and childhood height in the general population. 17767157 2007
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
0.010 GeneticVariation BEFREE The minor allele "C" of rs1042725 in HMGA2 was associated with an increased risk of CC in the allele, dominant and log-additive models. 27677077 2016
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
0.010 GeneticVariation BEFREE The minor allele "C" of rs1042725 in HMGA2 was associated with an increased risk of CC in the allele, dominant and log-additive models. 27677077 2016
cervical cancer
CUI: C4048328
Disease: cervical cancer
0.010 GeneticVariation BEFREE The minor allele "C" of rs1042725 in HMGA2 was associated with an increased risk of CC in the allele, dominant and log-additive models. 27677077 2016