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Table 2 Association and interaction between serum urate-associated single nucleotide polymorphisms and sex for gout risk

From: Interactions between serum urate-associated genetic variants and sex on gout risk: analysis of the UK Biobank

Gene

SNP

Effect allele

Women

n = 188,221

Men

n = 171,655

Gene-sex interaction

P

Effect allele absent

Referent OR

Effect allele present

OR (95% CI)

Effect allele absent

OR (95% CI)

Effect allele present

OR (95% CI)

Loci replicated by Kottgen

ABCG2

rs2231142

T

1

1.62 (1.35–1.94)

11.99 (10.81–13.30)

28.65 (25.73–31.90)

4.59 × 10−5

SLC2A9

rs12498742

A

1

4.12 (2.05–8.30)

18.09 (8.85–36.98)

55.62 (27.77–111.37)

0.42

GCKR

rs1260326

T

1

1.42 (1.18–1.70)

13.80 (11.77–16.18)

19.08 (16.33–22.29)

0.80

SLC17A3

rs1165151

T

1

0.76 (0.64–0.91)

13.15 (11.38–15.20)

10.56 (9.16–12.17)

0.60

SLC22A12

rs478607

A

1

0.78 (0.48–1.28)

13.96 (8.44–23.09)

10.57 (6.53–17.11)

0.90

PDZK1

rs1471633

A

1

0.92 (0.77–1.10)

10.54 (9.00–12.34)

13.61 (11.68–15.85)

3.67 × 10−4

INHBE

rs3741414

T

1

0.82 (0.69–0.98)

13.57 (12.16–15.15)

11.06 (9.89–12.38)

0.92

SLC16A9

rs1171614

T

1

0.95 (0.80–1.12)

14.28 (12.78–15.96)

11.74 (10.48–13.16)

0.11

SLC22A11

rs2078267

T

1

0.78 (0.65–0.95)

13.59 (11.42–16.17)

10.57 (8.93–12.51)

0.96

RREB1

rs675209

T

1

1.23 (1.04–1.45)

14.28 (12.62–16.16)

15.74 (13.90–17.82)

0.23

Loci reported by Kottgen

PKLR

rs11264341

T

1

0.82 (0.69–0.97)

13.09 (11.4–15.08)

11.34 (9.87–13.02)

0.57

INHBB

rs17050272

A

1

1.10 (0.93–1.32)

14.25 (12.26–16.57)

14.54 (12.54–16.85)

0.40

ACVR2A

rs2307394

T

1

0.99 (0.75–1.31)

14.72 (11.13–19.48)

13.28 (10.14–17.40)

0.53

MUSTN1

rs6770152

T

1

0.96 (0.78–1.19)

15.29 (12.50–18.70)

12.75 (10.49–15.51)

0.21

TMEM171

rs17632159

C

1

0.76 (0.65–0.90)

12.81 (11.39–14.41)

11.31 (10.06–12.73)

0.11

VEGFA

rs729761

T

1

0.99 (0.84–1.17)

13.89 (12.29–15.70)

13.03 (11.53–14.74)

0.55

MLXIPL

rs1178977

A

1

1.71 (1.00–2.90)

17.96 (10.42–30.95)

22.86 (13.50–38.72)

0.30

PRKAG2

rs10480300

T

1

0.97 (0.82–1.15)

12.74 (11.31–14.35)

14.07 (12.50–15.85)

0.15

STC1

rs17786744

A

1

1.36 (1.06–1.74)

17.59 (13.86–22.33)

17.64 (13.99–22.25)

0.02

HNF4G

rs2941484

T

1

1.11 (0.92–1.33)

14.00 (11.89–16.49)

14.78 (12.59–17.34)

0.62

ASAH2

rs10821905

A

1

0.96 (0.80–1.15)

12.86 (11.57–14.29)

14.63 (13.12–16.33)

0.07

LTBP3

rs642803

T

1

0.92 (0.77–1.10)

13.81 (11.80–16.16)

12.33 (10.58–14.38)

0.76

PTPN11

rs653178

T

1

0.85 (0.70–1.02)

13.30 (11.24–15.74)

11.52 (9.78–13.57)

0.82

NRG4

rs1394125

A

1

1.02 (0.86–1.21)

13.06 (11.40–14.98)

14.17 (12.38–16.21)

0.52

IGF1R

rs6598541

A

1

1.06 (0.89–1.25)

13.05 (11.38–14.96)

14.48 (12.65–16.56)

0.59

NFAT5

rs7193778

T

1

1.12 (0.63–1.98)

20.20 (11.23–36.35)

14.91 (8.44–26.35)

0.17

MAF

rs7188445

A

1

0.96 (0.82–1.14)

13.64 (12.01–15.48)

12.91 (11.38–14.65)

0.84

HLF

rs7224610

A

1

0.90 (0.72–1.12)

13.76 (11.13–17.00)

12.13 (9.89–14.89)

0.88

C17ORF82

rs2079742

T

1

0.92 (0.52–1.64)

10.34 (5.65–18.93)

12.54 (7.09–22.19)

0.38

PRPSAP1

rs164009

A

1

1.32 (1.02–1.71)

17.00 (13.25–21.82)

17.27 (13.55–22.01)

0.05

  1. Association and interaction data are reported according to effect allele presence or absence
  2. Data are adjusted by age, body mass index, diuretic use, and renal failure
  3. Experiment-wide significance is defined as P < 0.0017
  4. CI confidence interval, OR odds ratio, SNP single nucleotide polymorphism