rs143445068
This is a intron variant variant in the NAV2 gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
fertility trait
Laisk T et al. “The genetic architecture of sporadic and multiple consecutive miscarriage.” Nature Communications 11(1):5980 (2020)
Allele C
OR 3.43
p 5.0e-9
N 150,965
Large GWAS
European
About NAV2
This gene encodes a member of the neuron navigator gene family, which may play a role in cellular growth and migration. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]
View all NAV2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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