rs11723621

This is a intron variant variant in the GC gene.

GWAS Catalog Trait Associations (5)

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

vitamin D level

Manousaki D et al. Genome-wide Association Study for Vitamin D Levels Reveals 69 Independent Loci. American Journal of Human Genetics 106(3):327-337 (2020)
Allele G
OR 0.19
p
N 443,734
Large GWAS
European
Allele G
OR 0.15
p 1.0e-35
N 38,000
Large GWAS
South Asian

myeloid leukocyte count

Allele G
OR 0.03
p 8.0e-47
N 562,243
Large GWAS
European
Allele G
OR 0.03
p 5.0e-11
N 169,219
Large GWAS
European

neutrophil count

Allele G
OR 0.03
p 3.0e-37
N 519,288
Large GWAS
European
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 0.02
p 2.0e-24
N 432,666
Large GWAS
multi-ancestry
Allele G
OR 0.02
p 7.0e-24
N 394,642
Large GWAS
European

leukocyte quantity

Allele A
OR 0.02
p 2.0e-34
N 928,679
Large GWAS
multi-ancestry
Allele A
OR 0.03
p 2.0e-11
N 172,435
Large GWAS
European

monocyte count

Allele G
OR 0.01
p 1.0e-10
N 521,594
Large GWAS
European

About GC

The protein encoded by this gene belongs to the albumin gene family. It is a multifunctional protein found in plasma, ascitic fluid, cerebrospinal fluid and on the surface of many cell types. It binds to vitamin D and its plasma metabolites and transports them to target tissues. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Feb 2011]

View all GC variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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