rs6472846
This is a intron variant variant in the GDAP1 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.
gestational age
Solé-Navais P et al. “Genetic effects on the timing of parturition and links to fetal birth weight.” Nature Genetics 55(4):559-567 (2023)
Allele G
OR 0.35
p 1.0e-13
N 195,555
Large GWAS
European
About GDAP1
This gene encodes a member of the ganglioside-induced differentiation-associated protein family, which may play a role in a signal transduction pathway during neuronal development. Mutations in this gene have been associated with various forms of Charcot-Marie-Tooth Disease and neuropathy. Two transcript variants encoding different isoforms and a noncoding variant have been identified for this gene. [provided by RefSeq, Feb 2012]
View all GDAP1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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