Table 3 MR-MEGA fine-mapping results for loci with a single SNP within the 95% credible set

From: Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease

Locus

Number of significant SNPs

Nominated variant

CHR:BP:A1:A2

Nearest gene

Known PD gene ± 1 MB

Functional consequence

CADD

RDB

11

6

rs57891859

2:135464616:A:G

TMEM163

TMEM163

intronic

6.746

4

19

926

rs34311866

4:951947:C:T

TMEM175

TMEM175

exonic

11.09

NA

23

1483

rs356182

4:90626111:A:G

SNCA

SNCA

ncRNA intronic

8.962

NA

24

121

rs13117519

4:114369065:T:C

CAMK2D

CAMK2D

intergenic

1.216

3a

45

1371

rs10847864

12:123326598:G:T

HIP1R

HIP1R

intronic

2.403

2b

60

1

rs55818311

19:2341047:C:T

SPPL2B

LSM7

ncRNA exonic

1.096

5

  1. Known PD genes are either known PD risk genes (SNCA and TMEM175) or genes with the highest score in the nearest known PD locus by the PD GWAS Locus Browser37. CHR, chromosome; BP, base pair; A1, effect allele; A2, other allele; CADD, combined annotation-dependent depletion score; RDB, regulomeDB score; ncRNA, non-coding RNA.