rs34664882

This variant is located in the ANK1 gene.

GWAS Catalog Trait Associations (9)

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

mean reticulocyte volume

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele A
OR 0.24
p 1.0e-239
N 408,112
Large GWAS
European

erythrocyte volume

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele A
OR 0.23
p 4.0e-207
N 408,112
Large GWAS
European

reticulocyte count

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele A
OR 0.17
p 3.0e-149
N 408,112
Large GWAS
European

reticulocyte amount

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele A
OR 0.16
p 2.0e-140
N 408,112
Large GWAS
European

HbA1c 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 A
OR 0.15
p 3.0e-113
N 338,919
Major Consortium StudyLarge GWAS
multi-ancestry
Allele A
OR 0.05
p 2.0e-39
N 144,060
Large GWAS
multi-ancestry

mean corpuscular hemoglobin concentration

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele A
OR 0.16
p 7.0e-68
N 408,112
Large GWAS
European
Allele A
OR 0.13
p 4.0e-43
N 172,851
Large GWAS
European

bilirubin 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 A
OR 0.07
p 4.0e-28
N 354,368
Major Consortium StudyLarge GWAS
multi-ancestry

hemoglobin measurement

Allele A
OR
β 0.044
p 6.0e-14
N 684,122
Large GWAS
European

lymphocyte count

Allele A
OR 0.06
p 9.0e-11
N 171,643
Large GWAS
European

ClinVar annotation

Likely Benign★★★
8 submitters2 publications

not specified; Hereditary spherocytosis type 1; Spherocytosis; not provided; Sarcoma; Ovarian serous cystadenocarcinoma; Nonpapillary renal cell carcinoma; Familial pancreatic carcinoma; Colorectal cancer; Thyroid cancer, nonmedullary, 1; Melanoma; Acute myeloid leukemia; Hepatocellular carcinoma; Gastric cancer; Uterine carcinosarcoma; Malignant tumor of esophagus

View on ClinVar →

About ANK1

Ankyrins are a family of proteins that link the integral membrane proteins to the underlying spectrin-actin cytoskeleton and play key roles in activities such as cell motility, activation, proliferation, contact and the maintenance of specialized membrane domains. Multiple isoforms of ankyrin with different affinities for various target proteins are expressed in a tissue-specific, developmentally regulated manner. Most ankyrins are typically composed of three structural domains: an amino-terminal domain containing multiple ankyrin repeats; a central region with a highly conserved spectrin binding domain; and a carboxy-terminal regulatory domain which is the least conserved and subject to variation. Ankyrin 1, the prototype of this family, was first discovered in the erythrocytes, but since has also been found in brain and muscles. Mutations in erythrocytic ankyrin 1 have been associated in approximately half of all patients with hereditary spherocytosis. Complex patterns of alternative splicing in the regulatory domain, giving rise to different isoforms of ankyrin 1 have been described. Truncated muscle-specific isoforms of ankyrin 1 resulting from usage of an alternate promoter have also been identified. [provided by RefSeq, Dec 2008]

View all ANK1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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