rs1458038
This is a intergenic variant variant in the LOC124900725 gene.
▶GWAS Catalog Trait Associations (97)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (97)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
hematocrit
Chen MH et al. “Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.” Cell 182(5):1198-1213.e14 (2020)
Allele T
OR 0.02
p 1.0e-32
N 562,259
Large GWAS
European
Verma A et al. “Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.” Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele T
OR 0.02
p 1.0e-12
N 407,852
Major Consortium StudyLarge GWAS
European
serum creatinine amount
Verma A et al. “Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.” Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele C
OR 0.03
p 4.0e-28
N 600,139
Major Consortium StudyLarge GWAS
multi-ancestry
mean arterial pressure
Takeuchi F et al. “Interethnic analyses of blood pressure loci in populations of East Asian and European descent.” Nature Communications 9(1):5052 (2018)
Allele T
OR 0.60
p 4.0e-27
N 130,777
Large GWAS
multi-ancestry
Wain LV et al. “Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.” Nature Genetics 43(10):1005-11 (2011)
Allele T
OR 0.40
p 3.0e-14
N 74,064
Large GWAS
European
Sofer T et al. “Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos.” Scientific Reports 7(1):10348 (2017)
Allele T
OR 0.97
p 5.0e-8
N 12,278
Large GWAS
multi-ancestry
systolic blood pressure
Takeuchi F et al. “Interethnic analyses of blood pressure loci in populations of East Asian and European descent.” Nature Communications 9(1):5052 (2018)
Allele T
OR 0.84
p 3.0e-26
N 130,777
Large GWAS
multi-ancestry
Ehret GB et al. “The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.” Nature Genetics 48(10):1171-1184 (2016)
Allele T
OR 0.66
p 5.0e-24
N 201,529
Large GWAS
European
Wain LV et al. “Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.” Hypertension (dallas, Tex. : 1979) 70(3):e4-e19 (2017)
Allele T
OR 0.66
p 1.0e-16
N 150,134
Large GWAS
multi-ancestry
Kato N et al. “Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.” Nature Genetics 47(11):1282-1293 (2015)
Allele T
OR 0.97
p 5.0e-8
N 99,994
Large GWAS
multi-ancestry
Ehret GB et al. “Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.” Nature 478(7367):103-9 (2011)
Allele T
OR 0.71
p 2.0e-23
N 69,395
Large GWAS
European
Franceschini N et al. “Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans.” Plos One 11(10):e0164132 (2016)
Allele T
OR 1.37
p 9.0e-10
N 38,450
Large GWAS
multi-ancestry
phospholipids in very small VLDL measurement
Zoodsma M et al. “A genetic map of human metabolism across the allele frequency spectrum.” Nature Genetics 57(10):2445-2455 (2025)
Allele T
OR 0.02
p 2.0e-22
N 450,015
Large GWAS
multi-ancestry
free cholesterol in very small VLDL measurement
Zoodsma M et al. “A genetic map of human metabolism across the allele frequency spectrum.” Nature Genetics 57(10):2445-2455 (2025)
Allele T
OR 0.02
p 3.0e-22
N 450,015
Large GWAS
multi-ancestry
hypertension
Jeong H et al. “Identifying Interactions between Dietary Sodium, Potassium, Sodium-Potassium Ratios, and FGF5 rs16998073 Variants and Their Associated Risk for Hypertension in Korean Adults.” Nutrients 12(7) (2020)
Allele T
OR 1.26
p 3.0e-22
N 17,736
Large GWAS
East Asian
Takeuchi F et al. “Interethnic analyses of blood pressure loci in populations of East Asian and European descent.” Nature Communications 9(1):5052 (2018)
Allele T
OR 0.13
p 2.0e-20
N 50,792
Large GWAS
multi-ancestry
total lipids in very small VLDL measurement
Zoodsma M et al. “A genetic map of human metabolism across the allele frequency spectrum.” Nature Genetics 57(10):2445-2455 (2025)
Allele T
OR 0.02
p 7.0e-22
N 450,015
Large GWAS
multi-ancestry
concentration of very small VLDL particles
Zoodsma M et al. “A genetic map of human metabolism across the allele frequency spectrum.” Nature Genetics 57(10):2445-2455 (2025)
Allele T
OR 0.02
p 1.0e-21
N 450,015
Large GWAS
multi-ancestry
apolipoprotein B measurement
Zoodsma M et al. “A genetic map of human metabolism across the allele frequency spectrum.” Nature Genetics 57(10):2445-2455 (2025)
Allele T
OR 0.02
p 1.0e-20
N 450,015
Large GWAS
multi-ancestry
Richardson TG et al. “Evaluating the relationship between circulating lipoprotein lipids and apolipoproteins with risk of coronary heart disease: A multivariable Mendelian randomisation analysis.” Plos Medicine 17(3):e1003062 (2020)
Allele T
OR 0.02
p 6.0e-13
N 439,214
Large GWAS
European
▶Research that mentions this SNP (1)
▶Genome-wide association study of endometrial cancer in E2C2AssociationN=23,420Immaculata De Vivo et al.(2014)· Human Genetics
Genome-wide association study of endometrial cancer in E2C2
AssociationN=23,420Immaculata De Vivo et al.(2014)· Human Genetics
Genome-wide association study of endometrial cancer (7,077 cases, 16,343 controls) identifying replication of the known HNF1B locus (rs4430796, OR=0.82, P=4.3×10⁻¹¹) and a novel genome-wide significant association at the RNASET2 locus (rs9459805, OR=1.19, P=1.11×10⁻⁵). A suggestive locus at PRLR (prolactin receptor) was also identified.
Traits studied:Endometrial cancerEndometrioid endometrial cancerSerous endometrial cancer
This variant is in our database but has no known associations or PRS memberships yet.
Gene information from NCBI Gene. Variant classifications from ClinVar.
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