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. 2018 Sep 3;35(10):1656–1670. doi: 10.1007/s12325-018-0781-2

Table 2.

SNPs investigated

Chr Gene No. of SNPs; valid (total) SNPs
1 PLA2G4A 5 (6) rs10489407, rs6695515, rs10798069, rs10737276, rs12144159, rs7414079
2 CREB1 2 (4) rs889895, rs6740584, rs2551922, rs2254137
3 CHL1 8 (10) rs1516338, rs1516340, rs4003413, rs17271940, rs17274531, rs9990005, rs331893, rs2272522, rs13078884, rs9841789
3 GSK3B 4 (5) rs2037547, rs2873950, rs1719895, rs6782799, rs1381841
5 HOMER1 8 (8) rs3822568, rs6872497, rs4455546, rs12657371, rs12514775, rs6893883, rs4132033, rs10042665
7 SP4 5 (5) rs2282888, rs2237304, rs10272006, rs12673091, rs9648275
7 NCAPG2 4 (4) rs10772, rs877279, rs12113120, rs4621754
7 NCAPG2-ESYT2a 2 (3) rs12668837, rs9801117, rs6459896
7 ESYT2 6 (6) rs2013, rs3763406, rs3816462, rs2788469, rs842446, rs13233513
7 ESYT2-WDR60a 2 (2) rs1039621, rs2657375
7 WDR60 6 (6) rs2657323, rs1188974, rs2788478, rs10275341, rs2527204, rs2657340
7 VIPR2 2 (2) rs3793222, rs2270313
8 PPP3CC 4 (4) rs1522248, rs10108011, rs7430, rs2249098
9 SIGMAR1 1 (2) rs12115673, rs10814130
11 BDNF 7 (7) rs1519480, rs7124442, rs6265, rs11030101, rs11030102, rs11030104, rs12273363
13 HTR2A 11 (12) rs7323441, rs6314, rs7997012, rs1923886, rs643627, rs2224721, rs582385, rs17288723, rs2296973, rs6313, rs6311, rs1328685
15 RORA 26 (27) rs10438338, rs7167685, rs1657792, rs8040067, rs11630262, rs339996, rs9806453, rs2553235, rs1020729, rs1871858, rs12900122, rs17204440, rs12913922, rs341382, rs1673319, rs8041466, rs1234805, rs12148149, rs11071570, rs4775340, rs2414687, rs7178442, rs1403737, rs17270745, rs809736, rs7177611, rs10519113
15 ST8SIA2 11 (12) rs3759917, rs2305561, rs3784723, rs3784722, rs4777989, rs11629679, rs7168443, rs2290492, rs8035760, rs11853992, rs17522085, rs2279447
21 S100B 7 (8) rs9983498, rs2839350, rs9722, rs2186358, rs2839364, rs2839365, rs3788266, rs2839366
22 TXNRD2 2 (2) rs4646310, rs2020917
22 COMT 6 (6) rs933271, rs5993883, rs740603, rs2239393, rs4680, rs174696

All the SNPs genotyped in the Korean sample are reported in this table. Valid SNPs are shown in bold; those that were excluded from the analyses in italics (for details see “Methods” section)

aSNPs in these rows were located between two genes and, according to NCBI SNP database (https://www.ncbi.nlm.nih.gov/snp/), may affect both