rs1337101

This variant is located in the LYPLAL1-AS1 gene.

GWAS Catalog Trait Associations (8)

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

triglyceride measurement

Allele T
OR 0.02
p 5.0e-27
N 1,320,016
Large GWAS
European

Umbilical hernia

Allele T
OR 1.24
p 2.0e-21
N 275,546
Major Consortium StudyLarge GWAS
European

body weight

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele G
OR 0.03
p 4.0e-14
N 371,333
Major Consortium StudyLarge GWAS
multi-ancestry

Inguinal hernia

Allele T
OR 1.09
p 3.0e-13
N 275,546
Major Consortium StudyLarge GWAS
European

serum gamma-glutamyl transferase measurement

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 0.01
p 9.0e-12
N 477,575
Large GWAS
multi-ancestry

glycine measurement

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele T
OR 0.01
p 6.0e-11
N 450,015
Large GWAS
multi-ancestry

femoral hernia

Allele T
OR 1.35
p 7.0e-9
N 275,546
Major Consortium StudyLarge GWAS
European

This variant is in our database but has no known associations or PRS memberships yet.

Gene information from NCBI Gene. Variant classifications from ClinVar.

Community Wiki

No community notes yet for this variant. Sign in to start one.

Comments

Sign in to join the discussion.

Loading comments…