<p>Genes included in the Meta-analyses Symbol Aliases Cytogenetic Accession ID Location SNCA -synuclein, PARK1, NACP; non A4 component of 4q21 GDB:439047</p><p> amyloid precursor, PD1; Parkinson disease, familial 1 4q21.3-q22 PARK2 Parkin, PDJ, AR-JP, Parkinson disease (autosomal 6q25.2-q27 GDB:6802742</p><p> recessive, juvenile) 2 DRD2 Dopamine receptor D2 11q22.2-q22.3 GDB:119852 DRD4 Dopamine receptor D4 11p15.5 GDB:127782 SLC6A3 dopamine transporter (DAT1), solute carrier family 6 5p15.3 GDB:132445</p><p>(neurotransmitter transporter, dopamine) member 3 MAOA monoamine oxidase A Xp11.23 GDB:120164 MAOB monoamine oxidase B Xp11.23 GDB:119377 COMT catechol-O-methyltransferase 22q11.21-q11.23 GDB:119795 NAT2 AAC2; arylamide acetylase 2 (N-acetyltransferase 2, 8p22 GDB:125365</p><p> isoniazid inactivation) APOE apolipoprotein E 19q13.2 GDB:119691 GSTT1 glutathione S-transferase theta 1 22q11.2 GDB:371704 GSTM1 GST1, glutathione S-transferase M1, MU, H-B 1p13.3 GDB:120020 GSTP1 GST3, glutathione S-transferase pi, fatty acid ethyl ester 11q13 GDB:120024</p><p> synthase III, FAEES3, PI GSTZ1 MAAI, glutathione S-transferase Zeta 1 (maleylacetoacetate 14q24.3 GDB:9956548</p><p> isomerase) MTTE tRNA glutamic acid (tRNAglu) mitochondria GDB:118926 MTND2 NADH dehydrogenase subunit 2 (complex I; ND2) mitochondria GDB:118912 The gene symbols indicate those approved by the HUGO Nomenclature Subcommittee.</p>