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Table 2 Association results of the top SNPs in the meta-analysis

From: Genome-wide association study of periodontal pocketing in Finnish adults

 

N

Chr

Position

SNP

Nearest gene (function)

GTEX

Effect allele

EAF

Beta (95% CI)

SE

P value

(a)

3245

1

79069409

rs187209330

IFI44L (intergenic)

 

G

0.015

− 0.55 (− 0.78; − 0.32)

0.12

1.81 × 10–6

2

201819623

rs867275005

ORC2 (intron)

 

GAATA

0.040

− 0.33 (− 0.47; − 0.19)

0.071

3.83 × 10–6

3

5859909

rs12494721

AC027119.1

 

T

0.14

0.18 (0.11; 0.26)

0.039

3.11 × 10–6

4

183159364

rs12508476

TENM3 (intron)

 

C

0.83

0.16 (0.096; 0.23)

0.034

2.01 × 10–6

7

75505491

rs56045460

RHBDD2 (upstream)

TMEM120A (skin)

A

0.088

− 0.23 (− 0.33; − 0.14)

0.049

2.17 × 10–6

7

37556237

rs1364731

ELMO1 (intergenic)

NME8 (skin, thyroid)

T

0.37

0.12 (0.070; 0.17)

0.026

3.92 × 10–6

9

6868737

rs77366980

KDM4C (intron)

KDM4C,GLDC (brain)

T

0.14

− 0.17 (− 0.25; − 0.10)

0.038

3.91 × 10–6

13

112056064

rs7324141

TEX29 (intergenic)

ARHGEF7 (nerve, blood, adipose)

A

0.50

− 0.12 (− 0.17; − 0.069)

0.025

2.34 × 10–6

(b)

2925

6

7452509

rs200392355

HNRNPLP1 (indel)

 

CT

0.46

0.14 (0.084; 0.20)

0.030

2.23 × 10–6

8

139663617

rs3923549

COL22A1 (intron)

 

G

0.91

− 0.21 (− 0.30; − 0.12)

0.045

3.01 × 10–6

10

72481095

rs72814570

ADAMTS14 (intron)

ADAMTS14 (skin, mucosa, fibroblasts)

A

0.23

− 0.16 (− 0.22; − 0.093)

0.032

1.10 × 10–6

14

91608044

rs147203970

C14orf159 (intron)

 

T

0.033

0.37 (0.22; 0.52)

0.075

8.06 × 10–7

15

59799643

rs16941452

FAM81A (intron)

 

G

0.022

− 0.45 (− 0.63; − 0.26)

0.096

3.24 × 10–6

(c)

2650

6

7452509

rs200392355

HNRNPLP1 (indel)

 

CT

0.46

0.16 (0.093; 0.22)

0.032

1.22 × 10–6

8

10958526

rs2409703

XKR6 (intron)

 

C

0.079

0.28 (0.16; 0.39)

0.058

1.61 × 10–6

15

76021782

rs11630851

ODF3L1 (downstream)

LMAN1L (colon), NRG4 (lung, pituitary)

T

0.067

0.30 (0.18;0.42)

0.061

9.39 × 10–7

20

13340138

rs4444613

BANF2 (intergenic)

ISM1 (brain)

A

0.087

− 0.28 (− 0.38; − 0.18)

0.053

1.35 × 10–7

20

37763743

rs2003705

RP11-101E14.3 (intergenic)

DHX35 (colon, oesophagus, testis), FAM83D (artery, colon, oesophagus, skin), RP4-616B8.5 (oesophagus)

T

0.20

− 0.16 (− 0.23; − 0.097)

0.034

1.68 × 10–6

  1. N, number of participants; Chr, chromosome; SNP, variant identifier; Beta, effect estimate (unit is the number of affected teeth); EAF, effect allele frequency; SE, standard error; GTEX, genotype-tissue expression (GTEX-portal); Adjustments (a) Age, sex, and the first ten principal components, (b) Age, sex, smoking status, and the first ten principal components, (c) Age, sex, smoking status, plaque, and the first ten principal components. Reference genome: GRCh37