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. 2014 Jun 30;6(6):48. doi: 10.1186/gm566

Table 1.

Genomic loci implicated in Parkinson’s disease by genome-wide association analyses

Gene Chr Associated
SNP/locus
Genes within locus a Odds ratio
[95% CI]
P -value
GBA
1q21
N370S
TRIM46, MUC1, MIR92B, THBS3, GBAP1-GBA-FAM189B, SCAMP3, CLK2, HCN3, PKLR
3.37
[2.67-4.29]
1.11E-24
SYT11/RAB25
1q21
chr1:154105678
MIR7851, UBQLN4, LAMTOR2-RAB25-MEX3A, LMNA
1.67
[1.41-1.98]
5.70E-09
PM20D1
1q32
rs11240572
NUCK1-RAB7L1-SLC41A1, PM20D1
0.74
[0.69-0.80]
1.01E-14
STK39
2q24
rs2102808
STK39
1.28
[1.19-1.38]
1.54E-11
MCCC1/LAMP3
3q27
rs11711441
MCCC1-LAMP3-MCF2L2
0.84
[0.80-0.89]
8.72E-12
BST1
4p15
rs4698412
FAM200B-BST1
0.87
[0.83-0.91]
2.28E-10
GAK/DGKQ
4p16
rs1564282
CPLX1-GAK-TMEM175-DGKQ-SLC26A1, IDUA, FGFRL1
1.29
[1.20-1.38]
6.54E-13
SNCA
4q21
rs356220
SNCA-MMRN1
1.30
[1.25-1.34]
3.06E-49
HLA-DRB5
6p21
rs2395163
HLA-DRB5-HLA-DRB1, HLA-DRB6
0.75
[0.68-0.84]
2.90E-07
GPNMB
7p15
rs156429
GPNMB-MALSU1-IGF2BP3
0.89
[0.86-0.93]
2.69E-10
LRRK2
12q12
rs34778348
SLC2A13-LRRK2-MUC19, CNTN1
2.23
[1.89-2.63]
2.97E-21
CCDC62/HIP1R
12q24
rs12817488
DENR-HIP1R-VPS37B, ABCB9, OGFOD2,
1.17
[1.09-1.25]
2.99E-06
MAPT/STH 17q21 H1H2, 900kb inversion ARHGAP27, PLEKHM1, CRHR1, SPPL2C-MAPT-STH, KANSL1, LRRC37A, NSFP1, ARL17A/B 0.78
[0.75-0.80]
3.54E-52

Chr, chromosomal band; CI, confidence interval. aGenes within 100 kb of the most significantly associated SNP annotated from the UCSC genome browser (hg19). Odds ratios and P-values are the most significant findings from the PDGene database [150].