rs1886654

This is a coding sequence variant variant in the LINC02768 gene.

GWAS Catalog Trait Associations (14)

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

neutrophil measurement

Allele C
OR 0.22
p 7.0e-87
N 38,341
Large GWAS
European

monocyte count

Kachuri L et al. Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. American Journal of Human Genetics 108(10):1823-1835 (2021)
Allele T
OR
p 4.0e-71
N 234,690
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 0.05
p 6.0e-18
N 259,608
Major Consortium StudyLarge GWAS
European

leukocyte quantity

Allele T
OR 0.06
p 9.0e-60
N 928,679
Large GWAS
multi-ancestry
Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele T
OR 0.05
p 1.0e-46
N 504,825
Large GWAS
multi-ancestry
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 0.07
p 2.0e-49
N 381,099
Major Consortium StudyLarge GWAS
European

basophil count

Allele T
OR 0.05
p 2.0e-42
N 404,717
Large GWAS
European
Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele T
OR 0.04
p 3.0e-40
N 441,764
Large GWAS
multi-ancestry

C-type lectin domain family 4 member D measurement

Allele C
OR 0.07
p 4.0e-19
N 47,745
Large GWAS
European

matrix metalloproteinase-9 measurement

Allele C
OR 0.08
p 2.0e-17
N 47,745
Large GWAS
European

lymphocyte percentage of leukocytes

Allele C
OR 0.03
p 7.0e-17
N 394,642
Large GWAS
European

neutrophil percentage of leukocytes

Allele C
OR 0.03
p 7.0e-15
N 394,642
Large GWAS
European

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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