rs34225933
This variant is located in the F12;SLC34A1 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.
sulfate measurement
Yin X et al. “Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci.” Nature Communications 13(1):1644 (2022)
Allele T
OR 0.36
p 4.0e-13
N 6,136
Large GWAS
European
▶ClinVar annotation
Likely Benign★★★☆
7 submitters4 publicationsHereditary angioneurotic edema; Factor XII deficiency disease; Nephrolithiasis/osteoporosis, hypophosphatemic; not provided; Hypophosphatemic nephrolithiasis/osteoporosis 1; not specified
View on ClinVar →This variant is in our database but has no known associations or PRS memberships yet.
Gene information from NCBI Gene. Variant classifications from ClinVar.
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