rs6026578

This variant is located in the GNAS gene.

GWAS Catalog Trait Associations (8)

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

serum creatinine amount

Allele C
OR 0.02
p 6.0e-34
N 928,679
Large GWAS
multi-ancestry
Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele C
OR 0.02
p 4.0e-11
N 150,266
Large GWAS
East Asian

body height

Allele C
OR 0.01
p 2.0e-23
N 405,540
Large GWAS
European

appendicular lean mass

Allele C
OR 0.01
p 3.0e-14
N 450,243
Major Consortium StudyLarge GWAS
European

base metabolic rate measurement

Allele G
OR 0.01
p 4.0e-12
N 394,642
Large GWAS
European

uric acid measurement

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele G
OR 0.03
p 7.0e-12
N 129,405
Large GWAS
East Asian
Allele G
OR 0.03
p 5.0e-10
N 121,745
Meta-analysisLarge GWAS
multi-ancestry

diastolic blood pressure

Allele G
OR 0.11
p 2.0e-11
N 1,028,980
Large GWAS
multi-ancestry

urate measurement

Allele C
OR 0.04
p 8.0e-10
N 457,690
Large GWAS
multi-ancestry

health trait

Allele C
OR 0.01
p 4.0e-9
N 405,979
Large GWAS
European

About GNAS

This locus has a highly complex imprinted expression pattern. It gives rise to maternally, paternally, and biallelically expressed transcripts that are derived from four alternative promoters and 5' exons. Some transcripts contain a differentially methylated region (DMR) at their 5' exons, and this DMR is commonly found in imprinted genes and correlates with transcript expression. An antisense transcript is produced from an overlapping locus on the opposite strand. One of the transcripts produced from this locus, and the antisense transcript, are paternally expressed noncoding RNAs, and may regulate imprinting in this region. In addition, one of the transcripts contains a second overlapping ORF, which encodes a structurally unrelated protein - Alex. Alternative splicing of downstream exons is also observed, which results in different forms of the stimulatory G-protein alpha subunit, a key element of the classical signal transduction pathway linking receptor-ligand interactions with the activation of adenylyl cyclase and a variety of cellular reponses. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene result in pseudohypoparathyroidism type 1a, pseudohypoparathyroidism type 1b, Albright hereditary osteodystrophy, pseudopseudohypoparathyroidism, McCune-Albright syndrome, progressive osseus heteroplasia, polyostotic fibrous dysplasia of bone, and some pituitary tumors. [provided by RefSeq, Aug 2012]

View all GNAS 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…