rs34848191

This is a intron variant variant in the SPECC1 gene.

GWAS Catalog Trait Associations (5)

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

mean corpuscular hemoglobin

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 5.0e-71
N 478,500
Large GWAS
multi-ancestry
Allele T
OR 0.05
p 6.0e-39
N 172,332
Large GWAS
European

erythrocyte volume

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 5.0e-68
N 480,305
Large GWAS
multi-ancestry

red blood cell density

Allele T
OR
p 3.0e-22
N 727,624
Large GWAS
multi-ancestry

erythrocyte attribute

Allele T
OR 0.05
p 1.0e-14
N 38,277
Large GWAS
European

hemoglobin measurement

Allele T
OR 0.05
p 9.0e-14
N 39,127
Large GWAS
European

About SPECC1

The protein encoded by this gene belongs to the cytospin-A family. It is localized in the nucleus, and highly expressed in testis and some cancer cell lines. A chromosomal translocation involving this gene and platelet-derived growth factor receptor, beta gene (PDGFRB) may be a cause of juvenile myelomonocytic leukemia. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]

View all SPECC1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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