rs34311235
This is a intron variant variant in the LRP1B gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
motion sickness
Hromatka BS et al. “Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.” Human Molecular Genetics 24(9):2700-8 (2015)
Allele T
OR 0.03
p 8.0e-9
N 80,494
Large GWAS
European
About LRP1B
This gene encodes a member of the low density lipoprotein (LDL) receptor family. These receptors play a wide variety of roles in normal cell function and development due to their interactions with multiple ligands. Disruption of this gene has been reported in several types of cancer. [provided by RefSeq, Jun 2016]
View all LRP1B variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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