Table 2 Association analysis between SNPs and Parkinson’s disease.

From: Association of ARNTL and PER1 genes with Parkinson's disease: a case-control study of Han Chinese

Gene

SNPa

allele A>Bb

case

control

MAF

P-value

OR (95% CI)e

AA/AB/BBb

AA/AB/BBb

Trendc (bonferronif)

LRd (bonferronif)

NPAS2

rs930309

T>A

307/647/425

226/661/444

0.438

4.07 × 10−3

6.18 × 10−3

0.85 (0.77–0.95)

NPAS2

rs12479086

G>A

1031/315/37

1049/268/15

0.127

1.67 × 10−3

1.51 × 10−3

1.30 (1.11–1.53)

CLOCK

rs3749474

G>A

195/663/535

165/603/569

0.364

2.56 × 10−2

2.88 × 10−2

0.88 (0.79–0.98)

RORB

rs17611535

G>A

1140/237/14

1042/273/24

0.107

3.72 × 10−3

4.02 × 10−3

0.77 (0.65–0.92)

ARNTL

rs900147

G>A

289/715/369

233/612/455

0.444

3.33 × 10−5 (4.23 × 10−3)

5.13 × 10−5 (6.52 × 10−3)

0.80 (0.71–0.89)

ARNTL

rs7950226

G>A

447/704/238

493/639/198

0.407

8.84 × 10−3

6.84 × 10−3

0.86 (0.77–0.96)

ARNTL

rs11605776

C>A

365/675/349

290/667/377

0.487

4.91 × 10−3

6.02 × 10−3

0.86 (0.77–0.95)

ARNTL

rs10832022

A>G

405/683/299

435/666/232

0.443

4.77 × 10−3

7.16 × 10−3

1.17 (1.05–1.30)

ARNTL

rs11022765

C>A

501/667/222

541/615/175

0.382

4.85 × 10−3

6.99 × 10−3

1.17 (1.05–1.31)

ARNTL

rs1562437

G>A

39/421/926

52/463/809

0.197

1.33 × 10−3

1.36 × 10−3

0.81 (0.70–0.92)

PER1

rs2253820

A>G

630/632/121

711/501/88

0.289

5.30 × 10−6 (6.73 × 10−4)

1.37 × 10−5 (1.74 × 10−3)

1.31 (1.17–1.48)

NR1D1

rs3744805

G>A

231/610/512

245/646/409

0.416

2.94 × 10−3

2.43 × 10−3

1.18 (1.06–1.32)

  1. SNP, single nucleotide polymorphism; MAF, minor allele frequency; OR, odds ratio; CI, confidence interval, LR, logistic regression.
  2. aOnly SNPs with a P-value < 0.01 under the trend model are shown.
  3. bA allele is ancestral allele and B allele is alternative allele.
  4. cAsymptotic P-value.
  5. dWith age and sex as covariates.
  6. eOdds ratio under Cochran-Armitage trend model with 95% confidence interval.
  7. fBonferroni P-value (P-value × 125 tests).