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Table 1 Parkinson's disease associated risk SNPs from an East Asian meta-genome-wide association study (Foo et al. [20])

From: Evaluation of low-pass genome sequencing in polygenic risk score calculation for Parkinson’s disease

rs ID

Chromosome

Position

Effect allele

Featurea

Effect allele frequency

gnomAD v3.1 ALL

gnomAD v3.1 EAS

NARD ALL

NARD KOR

rs823118

1

205,723,572

T

EUR replicated

45.7%

54.3%

51.4%

52.5%

rs6679073

1

205,756,484

A

EAS

22.0%

53.3%

49.7%

51.2%

rs16846351

1

226,846,712

G

EAS

1.6%

6.3%

6.0%

6.4%

rs4653767

1

226,916,078

T

EUR replicated

72.7%

72.1%

23.8%

22.2%

rs2292056

3

182,735,211

T

EAS

77.9%

41.5%

59.9%

63.1%

rs12637471

3

182,762,437

G

EUR replicated

75.3%

42.0%

59.9%

62.9%

rs34311866

4

951,947

C

EUR replicated

14.2%

13.8%

17.7%

16.9%

rs11724635

4

15,737,101

A

EUR replicated

43.5%

37.5%

36.9%

34.3%

rs3816248

4

77,101,068

T

EAS

86.6%

66.1%

32.5%

33.4%

rs356182

4

90,626,111

G

EUR replicated

35.2%

66.2%

31.6%

29.1%

rs6826785

4

90,682,474

C

EAS

21.7%

54.8%

54.7%

55.5%

rs246814

5

75,599,208

T

EAS

9.6%

9.1%

NA

NA

rs1887316

6

112,151,452

G

EAS

81.1%

87.9%

12.4%

14.2%

rs997368

6

112,243,291

A

EUR replicated

65.5%

64.2%

39.3%

39.6%

rs9638616

7

70,750,493

T

EAS

37.9%

49.2%

55.0%

55.1%

rs12278023

11

83,510,117

T

EAS

55.1%

50.2%

47.7%

48.6%

rs3793947

11

83,544,472

G

EUR replicated

57.4%

53.4%

46.3%

47.0%

rs141336855

12

40,387,749

T

EAS

0.1%

2.6%

2.4%

2.4%

rs12456492

18

40,673,380

G

EUR replicated

32.8%

38.0%

42.7%

40.9%

rs4130047

18

40,678,235

C

EAS

32.2%

37.8%

42.6%

40.7%

  1. aFeature: EAS represents significant SNPs from this GWAS (P < 5.00 × 10–8); EUR replicated represents replicated SNPs in this GWAS (P < 1.00 × 10–5)