rs4316067

GWAS Catalog Trait Associations (9)

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

Red cell distribution width

Allele A
OR
p 1.0e-243
N 563,352
Large GWAS
multi-ancestry
Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele A
OR 0.06
p 3.0e-137
N 408,112
Large GWAS
European
Allele A
OR 0.06
p 4.0e-202
N 394,642
Large GWAS
European
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 A
OR 0.07
p 6.0e-121
N 380,796
Major Consortium StudyLarge GWAS
European
Allele A
OR 0.07
p 2.0e-62
N 116,666
Large GWAS
European

orotate measurement

Allele A
OR 0.24
p 3.0e-111
N 14,296
Large GWAS
European
Feofanova EV et al. Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations. Nature Communications 14(1):3111 (2023)
Allele A
OR 0.28
p 9.0e-79
N 9,243
Large GWAS
multi-ancestry
Allele A
OR 0.22
p 2.0e-42
N 8,809
Large GWAS
European
Allele A
OR 0.34
p 2.0e-95
N 8,128
Large GWAS
European
Allele A
OR 0.30
p 3.0e-49
N 6,136
Large GWAS
European

level of cytosolic 5'-nucleotidase 3A in blood

Allele G
OR 0.11
p 1.0e-64
N 47,745
Large GWAS
European

serum metabolite level

Allele A
OR 0.33
p 5.0e-48
N 3,926
Large GWAS
Hispanic or Latin American

uridine diphosphate measurement

Allele A
OR 0.87
p 3.0e-34
N 243
Small GWAS

orotic acid measurement

Allele G
OR 0.27
p 2.0e-19
N 2,466
Large GWAS
multi-ancestry

erythrocyte volume

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele G
OR 0.02
p 8.0e-15
N 408,112
Large GWAS
European

mean reticulocyte volume

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele G
OR 0.02
p 7.0e-10
N 408,112
Large GWAS
European

This variant is in our database but has no known associations or PRS memberships yet.

Gene information from NCBI Gene. Variant classifications from ClinVar.

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