rs12413946 (LINC02929): Blood Cell Trait Variant
Key takeaways
- rs12413946 lies near the LINC02929 gene and was identified in a large genome-wide study of blood cell traits.
- The study tested 36 hematological properties in 173,480 European-ancestry participants.
- Across all blood cell traits, 2,706 independently associated variants were found, including low-frequency and rare variants with stronger effects.
- Specific effect sizes or the exact blood cell trait linked to rs12413946 are not detailed in the available study text.
Key takeaways
- rs12413946 lies near the LINC02929 gene (a long intergenic non-coding RNA, meaning a gene that does not produce a protein) and was identified in a large genome-wide study of blood cell traits.
- The study tested 36 hematological properties - spanning red cells, white cells, and platelets - in 173,480 European-ancestry participants.
- Across all blood cell traits, 2,706 independently associated variants were found, including low-frequency and rare variants with stronger individual effects than common variants.
- Specific effect sizes or the exact blood cell trait linked to rs12413946 are not detailed in the available study text.
What the research says A genome-wide association study of 36 blood cell indices in 173,480 European-ancestry individuals from the UK Biobank and INTERVAL studies identified rs12413946 at this locus among thousands of variants associated with hematological traits. The study tested 29.5 million genetic variants and found 2,706 independently associated variants, including 130 rare (minor allele frequency under 1%) and 230 low-frequency (1%-5%) variants with notable impact on blood cell phenotypes. The authors applied Mendelian randomization - a statistical technique that uses genetic variants to estimate whether a trait causally influences a disease - to explore links between blood cell indices and complex diseases including autoimmune conditions, schizophrenia, and coronary heart disease.
Reported associations
- Blood cell traits (hematological indices): rs12413946 was identified as a variant associated with one or more of 36 blood cell properties in 173,480 European-ancestry participants from the UK Biobank and INTERVAL studies; the available study text does not specify which trait or the effect size for this individual variant.
Evidence quality The source study provides substantial statistical power with 173,480 participants and 29.5 million tested variants; rs12413946 is one of 2,706 independently associated signals identified. The available text does not report the specific p-value, effect size, or independent replication data for this variant alone. The study population is limited to individuals of European ancestry, which may affect how broadly the findings apply to other groups. Evidence for this specific variant should be considered preliminary until further targeted analyses are published.
Lifestyle considerations No lifestyle considerations on file for this variant.
Frequently asked questions
What is rs12413946?
rs12413946 is a genetic variant located near the LINC02929 gene, identified in a large genome-wide study of blood cell traits. It is one of thousands of variants found to be associated with red cell, white cell, or platelet properties in European-ancestry individuals.
What does the LINC02929 gene do?
LINC02929 stands for Long Intergenic Non-Coding RNA 2929, meaning it is a gene that does not produce a protein but may play a regulatory role. The research linking this region to blood cell traits is still emerging and the specific function of this RNA in blood biology is not yet established.
Is rs12413946 linked to blood disorders?
The study that identified rs12413946 tested associations with 36 blood cell properties in over 173,000 participants, but does not classify this variant as linked to a specific blood disorder. The exact trait and effect size for this variant are not fully detailed in the available study text.
How large was the study that identified this variant?
The study included 173,480 European-ancestry participants from the UK Biobank and INTERVAL studies, testing 29.5 million genetic variants across 36 blood cell traits.
Does rs12413946 affect individual health?
Population-level genetic studies cannot be used to determine individual health outcomes. The study identified rs12413946 in a group of over 173,000 people, but its specific implications for any one person are not established by the available research.