rs1043879

This is a protein-altering variant in the RSRP1 gene.

GWAS Catalog Trait Associations (4)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

apolipoprotein B measurement

Sinnott-Armstrong N et al. Genetics of 35 blood and urine biomarkers in the UK Biobank. Nature Genetics 53(2):185-194 (2021)
Allele C
OR 0.02
p 8.0e-17
N 354,097
Major Consortium StudyLarge GWAS
multi-ancestry

total cholesterol measurement

Sinnott-Armstrong N et al. Genetics of 35 blood and urine biomarkers in the UK Biobank. Nature Genetics 53(2):185-194 (2021)
Allele C
OR 0.02
p 8.0e-17
N 355,858
Major Consortium StudyLarge GWAS
multi-ancestry

low density lipoprotein cholesterol measurement

Sinnott-Armstrong N et al. Genetics of 35 blood and urine biomarkers in the UK Biobank. Nature Genetics 53(2):185-194 (2021)
Allele C
OR 0.02
p 7.0e-16
N 355,197
Major Consortium StudyLarge GWAS
multi-ancestry

mean corpuscular hemoglobin concentration

Allele C
OR 0.03
p 3.0e-13
N 172,851
Large GWAS
European

About RSRP1

Involved in spliceosomal complex assembly. Located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]

View all RSRP1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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