rs12473839

This is a intron variant variant in the ACMSD gene.

GWAS Catalog Trait Associations (7)

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

erythrocyte count

Allele T
OR 0.01
p 3.0e-17
N 394,642
Large GWAS
European
Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele T
OR 0.02
p 3.0e-11
N 408,112
Large GWAS
European

esterified cholesterol 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-13
N 450,015
Large GWAS
multi-ancestry

sphingomyelin 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 7.0e-13
N 450,015
Large GWAS
multi-ancestry

total cholesterol 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 9.0e-13
N 450,015
Large GWAS
multi-ancestry

low density lipoprotein cholesterol 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 3.0e-11
N 416,487
Large GWAS
multi-ancestry

red blood cell density

Allele T
OR
p 2.0e-15
N 727,624
Large GWAS
multi-ancestry

About ACMSD

The neuronal excitotoxin quinolinate is an intermediate in the de novo synthesis pathway of NAD from tryptophan, and has been implicated in the pathogenesis of several neurodegenerative disorders. Quinolinate is derived from alpha-amino-beta-carboxy-muconate-epsilon-semialdehyde (ACMS). ACMSD (ACMS decarboxylase; EC 4.1.1.45) can divert ACMS to a benign catabolite and thus prevent the accumulation of quinolinate from ACMS.[supplied by OMIM, Oct 2004]

View all ACMSD variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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