rs35467921

This is a intron variant variant in the TLCD3B gene.

GWAS Catalog Trait Associations (6)

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

base metabolic rate measurement

Allele T
OR 0.02
p 8.0e-66
N 394,642
Large GWAS
European

whole body water mass

Allele T
OR 0.02
p 3.0e-65
N 394,642
Large 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 C
OR 0.04
p 7.0e-43
N 288,216
Major Consortium StudyLarge GWAS
European

body mass index

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 C
OR 0.03
p 4.0e-34
N 424,217
Major Consortium StudyLarge GWAS
European

health trait

Allele C
OR 0.01
p 8.0e-20
N 405,979
Large GWAS
European

grip strength measurement

Allele C
OR 0.01
p 4.0e-10
N 404,112
Large GWAS
European

About TLCD3B

This gene encodes a transmembrane protein, which may be a likely target of peroxisome proliferator-activated receptor gamma (PPAR-gamma). The product of the orthologous gene in mouse is related to obesity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]

View all TLCD3B variants →

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…