rs6857

This is a upstream gene variant variant in the NECTIN2 gene.

GWAS Catalog Trait Associations (44)

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

protein measurement

Pietzner M et al. Mapping the proteo-genomic convergence of human diseases. Science (new York, N.y.) 374(6569):eabj1541 (2021)
Allele T
OR 0.74
p
N 10,708
Large GWAS
European
Allele T
OR 0.23
p 1.0e-13
N 2,721
Large GWAS
European

dementia

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 0.55
p 9.9e-324
N 443,046
Major Consortium StudyLarge GWAS
European

Alzheimer disease, family history of Alzheimer’s disease

Willett JDS et al. Identification of 16 novel Alzheimer's disease loci using multi-ancestry meta-analyses. Alzheimer's & Dementia : the Journal of the Alzheimer's Association 21(2):e14592 (2025)
Allele T
OR
p 2.0e-277
N 404,467
Large GWAS
multi-ancestry

Alzheimer disease

Willett JDS et al. Identification of 16 novel Alzheimer's disease loci using multi-ancestry meta-analyses. Alzheimer's & Dementia : the Journal of the Alzheimer's Association 21(2):e14592 (2025)
Allele T
OR
p 2.0e-189
N 27,907
Large GWAS
European, African unspecified, Hispanic or Latin American, Asian unspecified, NR
Jun GR et al. Transethnic genome-wide scan identifies novel Alzheimer's disease loci. Alzheimer's & Dementia : the Journal of the Alzheimer's Association 13(7):727-738 (2017)
Allele T
OR 3.22
p 7.0e-18
N 33,263
Large GWAS
multi-ancestry

amyloid-beta measurement

Allele T
OR 1.67
p 6.0e-132
N 4,314
Large GWAS
multi-ancestry

linoleic acid measurement

Allele T
OR
p 1.0e-120
N 239,268
Large GWAS
European
Karjalainen MK et al. Genome-wide characterization of circulating metabolic biomarkers. Nature 628(8006):130-138 (2024)
Allele T
OR 0.06
p 1.0e-15
N 70,413
Large GWAS
European

Research that mentions this SNP (2)

A Comprehensive Genetic Association Study of Alzheimer Disease in African Americans
AssociationN=1,009Logue MW et al.(2011)· Archives of Neurology

This comprehensive genome-wide association study examined genetic variants contributing to late-onset Alzheimer's disease (AD) in 513 African American cases and 496 controls, plus replication in 5 white cohorts. The APOE ε4 allele showed strong association (P=9.69×10⁻²³), and after adjusting for APOE, rs6859 in PVRL2 remained significantly associated (P=0.0087). The study found associations with variants in CLU, PICALM, BIN1, EPHA1, MS4A, ABCA7, and CD33, though effect directions sometimes differed from white populations. Novel associations with suggestive evidence were identified in PROX1, CNTNAP2, STK24, and other genes, though not replicated in whites.

Traits studied:Alzheimer diseaseLate-onset Alzheimer disease (LOAD)
Genome-wide Analysis of Genetic Loci Associated With Alzheimer Disease
AssociationN=35,000Seshadri S. et al.(2010)· JAMA

This 3-stage genome-wide association meta-analysis study identified 5 novel and confirmed loci associated with late-onset Alzheimer's disease across over 35,000 individuals. The study discovered two new genome-wide significant loci: rs744373 in BIN1 (OR 1.13, p=1.59×10⁻¹¹) and rs597668 near EXOC3L2 (OR 1.18, p=6.45×10⁻⁹), and confirmed three previously reported loci in APOE (OR 2.53, p=1.04×10⁻²⁹⁵), CLU (OR 0.85, p=1.62×10⁻¹⁶), and PICALM (OR 0.89, p=3.16×10⁻¹²). These findings were validated in an independent Spanish replication sample of 2,349 individuals.

Traits studied:Alzheimer's diseaseLate-onset Alzheimer's disease

About NECTIN2

This gene encodes a single-pass type I membrane glycoprotein with two Ig-like C2-type domains and an Ig-like V-type domain. This protein is one of the plasma membrane components of adherens junctions. It also serves as an entry for certain mutant strains of herpes simplex virus and pseudorabies virus, and it is involved in cell to cell spreading of these viruses. Variations in this gene have been associated with differences in the severity of multiple sclerosis. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]

View all NECTIN2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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