rs35667547

This variant is located in the ADAMTS9 gene.

GWAS Catalog Trait Associations (3)

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

retinal layer thickness

Jackson VE et al. Multi-omic spatial effects on high-resolution AI-derived retinal thickness. Nature Communications 16(1):1317 (2025)
Allele C
OR 0.48
p 2.0e-18
N 43,148
Large GWAS
multi-ancestry

diastolic blood pressure

Allele C
OR 0.15
p 6.0e-9
N 1,028,980
Large GWAS
multi-ancestry

glomerular filtration rate

Allele C
OR 5.71
p 1.0e-8
N 1,508,659
Large GWAS
multi-ancestry
Allele C
OR
β 0.019
p 3.0e-10
N 406,504
Large GWAS
European

ClinVar annotation

Benign★★★
2 submitters1 publication
View on ClinVar →

About ADAMTS9

This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. Members of the ADAMTS family have been implicated in the cleavage of proteoglycans, the control of organ shape during development, and the inhibition of angiogenesis. This gene is localized to chromosome 3p14.3-p14.2, an area known to be lost in hereditary renal tumors. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Jan 2016]

View all ADAMTS9 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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