rs62471615
This is a intron variant variant in the LINC-PINT gene.
▶GWAS Catalog Trait Associations (2)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (2)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
myeloproliferative disorder
Bao EL et al. “Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells.” Nature 586(7831):769-775 (2020)
Allele C
OR 1.30
p 7.0e-19
N 585,140
Large GWAS
European
lymphocyte count
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 0.02
p 7.0e-11
N 445,573
Large GWAS
multi-ancestry
About LINC-PINT
Involved in negative regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
View all LINC-PINT variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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