rs6568554
This is a intron variant variant in the ARMC2 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.
birth weight, parental genotype effect measurement
Warrington NM et al. “Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors.” Nature Genetics 51(5):804-814 (2019)
Allele A
OR 0.03
p 2.0e-9
N 230,069
Large GWAS
European
About ARMC2
Involved in sperm axoneme assembly. Implicated in spermatogenic failure 38. [provided by Alliance of Genome Resources, Jul 2025]
View all ARMC2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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