rs79744308

This variant is located in the NRTN gene.

GWAS Catalog Trait Associations (5)

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

lactoperoxidase measurement

Pietzner M et al. Mapping the proteo-genomic convergence of human diseases. Science (new York, N.y.) 374(6569):eabj1541 (2021)
Allele A
OR 0.57
p 9.0e-72
N 10,708
Large GWAS
European

blood protein amount

Allele A
OR 0.55
p 5.0e-25
N 5,364
Large GWAS
European

level of mucin-13 in blood

Allele A
OR 0.11
p 3.0e-16
N 47,745
Large GWAS
European

alkaline phosphatase measurement

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele A
OR 0.04
p 1.0e-15
N 463,178
Large GWAS
multi-ancestry

interleukin-1 receptor-like 2 measurement

Allele A
OR 0.09
p 3.0e-15
N 47,745
Large GWAS
European

ClinVar annotation

Benign★★★
2 submitters1 publication

not specified; not provided

View on ClinVar →

About NRTN

This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. The encoded preproprotein is proteolytically processed to generate the mature protein. This protein signals through the RET receptor tyrosine kinase and a GPI-linked coreceptor, and promotes survival of neuronal populations. A neurturin mutation has been described in a family with Hirschsprung Disease. [provided by RefSeq, Aug 2016]

View all NRTN variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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