rs4896582

This is a intron variant variant in the ADGRG6 gene.

GWAS Catalog Trait Associations (2)

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

body height

Allele A
OR 0.05
p 3.0e-55
N 253,288
Large GWAS
European
Allele A
OR 0.38
p 2.0e-18
N 15,821
Large GWAS
European

BMI-adjusted waist circumference

Allele A
OR 0.03
p 7.0e-18
N 219,872
Major Consortium StudyLarge GWAS
European
Allele A
OR 0.03
p 2.0e-8
N 122,328
Meta-analysisLarge GWAS
multi-ancestry

Research that mentions this SNP (1)

Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci
AssociationN=3,571Shu-Feng Lei et al.(2009)· Human Genetics

Genome-wide association study in 618 Northern Chinese and replication in 2,953 Southern Chinese identified 13 contiguous SNPs in the ZNF510/ZNF782 region significantly associated with stature (P = 9.71×10^-5 to 3.11×10^-6, FDR q = 0.036-0.046). The most significant SNP rs10816533 replicated in Southern Chinese (P = 0.029, combined P = 1.55×10^-6), suggesting this is an ethnic-specific locus for height variation in Chinese populations.

Traits studied:Adult heightHuman stature

About ADGRG6

This gene, which is upregulated in human umbilical vein endothelial cells, encodes a G protein-coupled receptor. Variations in this gene can affect a person's stature. Multiple transcript variants encoding different proteins have been found for this gene. [provided by RefSeq, Mar 2009]

View all ADGRG6 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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