rs1165195

This is a intron variant variant in the SLC17A1 gene.

GWAS Catalog Trait Associations (12)

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

metabolite measurement

Allele G
OR 0.35
p 2.0e-101
N 4,900
Large GWAS
European

hexanoylglutamine measurement

Allele G
OR 0.39
p 4.0e-85
N 4,808
Large GWAS
European
Allele G
OR 0.36
p 3.0e-69
N 6,136
Large GWAS
European

X-19141 measurement

Allele G
OR 0.36
p 1.0e-68
N 6,136
Large GWAS
European

X-24556 measurement

Allele G
OR 0.22
p 2.0e-47
N 8,004
Large GWAS
European
Allele G
OR 0.21
p 3.0e-27
N 6,136
Large GWAS
European

uric acid measurement

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele G
OR 0.07
p 5.0e-44
N 129,405
Large GWAS
East Asian

X-12822 measurement

Allele G
OR 0.27
p 2.0e-33
N 6,136
Large GWAS
European

X-25371 measurement

Allele G
OR 0.24
p 7.0e-33
N 6,136
Large GWAS
European

21-hydroxypregnenolone disulfate measurement

Allele G
OR 0.16
p 1.0e-28
N 8,132
Large GWAS
European

X-16087 measurement

Allele G
OR 0.23
p 3.0e-26
N 6,136
Large GWAS
European

X-21364 measurement

Allele G
OR 0.20
p 4.0e-22
N 6,136
Large GWAS
European
Allele G
OR 0.13
p 9.0e-18
N 8,203
Large GWAS
European

About SLC17A1

Predicted to enable transmembrane transporter activity. Involved in sodium-dependent phosphate transport; urate metabolic process; and urate transport. Located in apical plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]

View all SLC17A1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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