rs9389269

This is a upstream gene variant variant in the LOC105378010 gene.

GWAS Catalog Trait Associations (12)

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

hemoglobin measurement

Allele C
OR 0.21
p 9.0e-154
N 38,200
Large GWAS
European

erythrocyte attribute

Allele C
OR 0.16
p 4.0e-95
N 38,277
Large GWAS
European

erythrocyte count

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 T
OR 0.13
p 7.0e-74
N 55,750
Major Consortium StudyLarge GWAS
Hispanic or Latin American

platelet count

Allele C
OR 0.13
p 6.0e-41
N 72,816
Large GWAS
East Asian

deficiency anemia

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 T
OR 0.29
p 7.0e-32
N 624,264
Major Consortium StudyLarge GWAS
multi-ancestry

hyperlipidemia

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 T
OR 0.05
p 2.0e-17
N 426,603
Major Consortium StudyLarge GWAS
European

metabolic disease

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 T
OR 0.05
p 3.0e-17
N 426,570
Major Consortium StudyLarge GWAS
European

soluble transferrin receptor measurement

Allara E et al. Novel loci and biomedical consequences of iron homoeostasis variation. Communications Biology 7(1):1631 (2024)
Allele T
OR 0.06
p 3.0e-15
N 45,330
Large GWAS
European

guanine nucleotide exchange factor VAV3 measurement

Allele C
OR 0.05
p 1.0e-11
N 47,745
Large GWAS
European

ATP measurement

Allele C
OR 0.07
p 7.0e-10
N 11,334
Large GWAS
multi-ancestry

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

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…