rs1056930

This variant is located in the NRIP1 gene.

GWAS Catalog Trait Associations (3)

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

systolic blood pressure

Allele C
OR 0.17
p 4.0e-12
N 1,028,980
Large GWAS
multi-ancestry

pulse pressure measurement

Allele C
OR 0.12
p 8.0e-12
N 1,028,980
Large GWAS
multi-ancestry

body weight

Allele T
OR 0.01
p 5.0e-8
N 928,679
Large GWAS
multi-ancestry

About NRIP1

Nuclear receptor interacting protein 1 (NRIP1) is a nuclear protein that specifically interacts with the hormone-dependent activation domain AF2 of nuclear receptors. Also known as RIP140, this protein modulates transcriptional activity of the estrogen receptor. [provided by RefSeq, Jul 2008]

View all NRIP1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

Community Wiki

No community notes yet for this variant. Sign in to start one.

Comments

Sign in to join the discussion.

Loading comments…