Table 4 SLC2A9 sequence variants associated with serum urate (Top 10 significant associations reported here).

From: Fine mapping and identification of serum urate loci in American Indians: The Strong Heart Family Study

SNP*

Chr-pos hg19

Major/Minor Allele

MAF

P-value

β

SE

Effect Size

rs4481233

9956079

G/A

0.30

4.2 × 10−24

−0.35

0.03

0.05

rs11723439

9951819

G/A

0.28

1.5 × 10−23

−0.35

0.03

0.05

rs28592748

9998605

G/A

0.25

2.7 × 10−22

−0.35

0.04

0.05

rs7669607

9997801

G/A

0.25

8.2 × 10−22

−0.35

0.04

0.05

rs13111638

9996890

G/A

0.23

1.4 × 10−21

−0.36

0.04

0.05

rs10939650

9998440

A/G

0.35

4.1 × 10−21

−0.31

0.03

0.04

rs4529048

9997112

A/C

0.36

5.0 × 10−21

−0.31

0.03

0.04

rs3733588

9997303

A/G

0.35

7.3 × 10−21

−0.31

0.03

0.04

rs1014290

10001861

A/G

0.35

7.6 × 10−21

−0.31

0.03

0.04

rs4385059

9989233

A/G

0.23

3.6 × 10−20

−0.34

0.04

0.04

  1. *SNPs after accounting for linkage disequilibrium (LD; r2 ≥ 0.80); SNP: single nucleotide polymorphism; Chr pos: chromosome position in base pairs; MAF: minor allele frequency; P-value: P-values from measured genotype analysis; β: beta coefficient of the SNP; SE: standard error; Effect Size: Proportion of the residual phenotypic variance that is explained by the minor allele of the SNP; Gene loc: Gene location.
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