rs10412446

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

GWAS Catalog Trait Associations (4)

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

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 A
OR 0.04
p 5.0e-34
N 405,357
Major Consortium StudyLarge GWAS
European

hematocrit

Allele G
OR 0.02
p 1.0e-27
N 562,259
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 G
OR 0.02
p 4.0e-14
N 584,645
Major Consortium StudyLarge GWAS
multi-ancestry

body height

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 0.03
p 2.0e-13
N 607,510
Major Consortium StudyLarge GWAS
multi-ancestry
Allele A
OR 0.11
p 2.0e-8
N 283,749
Major Consortium StudyLarge GWAS
European

hemoglobin measurement

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 0.02
p 2.0e-15
N 584,680
Major Consortium StudyLarge GWAS
multi-ancestry

About NOSIP

The protein encoded by this gene may modulate the activity and localization of nitric oxide synthase (endothelial and neuronal) and thus nitric oxide production. Alternative splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Aug 2012]

View all NOSIP variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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