Table 2 Genomic risk loci for AAO identified in the genome-wide meta-analysis.

From: Common genetic variants contribute to heritability of age at onset of schizophrenia

Genomic Locus

Positiona

Lead SNP

Lead SNP position

P-value

nSNPsb

Genes

1

1:181854925

rs185188889

1:181854925

6.735e−06

1

2

2:81911239:82893571

rs13383639

82802994

7.8040E−06

19

REG3G, REG1B, REG3A, CTNNA2, LRRTM1, SUCLG1

3

3:173494302:173563936

rs7652242

173553275

4.57E−06

59

NLGN1, NAALADL2

4

4:30196116:30196116

rs111289733

30196116

1.66E−07

1

RP11-180C1.1

5

4:38573143:38604331

rs4833071

38582859

4.79E−06

12

RELL1, TBC1D1, PTTG2, AC021860.1, KLF3, TLR10, RFC1, UGDH

6

4:40443966:40443966

rs10755175

40443966

4.49E−06

1

RHOH, RBM47, NSUN7

7

4:167064039:167096817

rs10018884

167092502

2.36E−06

65

MARCH1, MSMO1, SPOCK3, ANXA10, DDX60, PALLD

8

5:108260989:108520863

rs78438786

108260989

6.72E−07

6

FER, PJA2, MAN2A1, TMEM232, SLC25A46

9

5:120718453:120901978

rs2195409

120892594

6.73E−06

34

DMXL1, HSD17B4, FAM170A, FTMT, SRFBP1, LOX, SNCAIP

10

5:133457000:133774168

rs4431386

133557876

2.54E−06

65

SLC22A5, C5orf56, IL4, KIF3A, CCNI2, GDF9, UQCRQ, LEAP2, AFF4, ZCCHC10, HSPA4, C5orf15, VDAC1, TCF7, SKP1, CTD-2410N18.5, PPP2CA, CDKL3, UBE2B, CDKN2AIPNL, JADE2, SAR1B, SEC24A, DDX46, C5orf24, TXNDC15, PCBD2, PITX1

11

7:48751259:48840965

rs139864446

48831950

9.07E−06

7

AC004899.1, VWC2, C7orf72, IKZF1, DDC

12

7:106206611:106399401

rs111513327

106207969

1.75E−06

7

EFCAB10, ATXN7L1, SYPL1, NAMPT, CCDC71L, PIK3CG, PRKAR2B, HBP1, COG5, DUS4L, BCAP29, SLC26A4, CBLL1, SLC26A3

13

8:20289797:20370404

rs12550821

20315601

4.85E−06

32

CSGALNACT1, LPL, SLC18A1, ATP6V1B2, LZTS1, GFRA2, DOK2, XPO7, LGI3, SFTPC, BMP1

14

8:121006828:121262332

rs10808509

121227216

5.61E−06

77

TAF2, DSCC1, DEPTOR, COL14A1, MRPL13, MTBP, SNTB1

15

11:2192798:2192798

rs10840489

2192798

2.04E−06

1

KRTAP5-4, KRTAP5-5, KRTAP5-6, IFITM10, RP11-295K3.1, CTSD, SYT8, TNNI2, LSP1, C11orf89, TNNT3, TH, C11orf21

16

11:44644743:44870058

rs11038082

44644743

2.51E−06

28

C11orf96, EXT2, ALX4, CD82, TSPAN18, TP53I11, PRDM11, SYT13, SLC35C1, CRY2

17

12:32500207:32537185

rs144642024

32500207

1.58E−06

2

OVCH1, FAM60A, AC024940.1, DENND5B, METTL20, AMN1, KIAA1551, FGD4, DNM1L, YARS2, ALG10

18

13:61356260:61390956

rs9570366

61377708

1.69E−06

19

PCDH20

19

14:20479798:20546983

rs72667672

20492904

6.82E−06

82

OR4N2, OR4K2, OR4K5, OR4K1, OR4K14, OR4K13, OR4L1, OR4K17, OR4N5, TTC5, RNASE9, RNASE4, ANG, AL163636.6

20

16:71388416:71388416

rs142248381

71388416

2.45E−07

1

COG4, SF3B3, MTSS1L, VAC14, HYDIN, CMTR2, ZNF23, ZNF19, TAT, HP, HPR

21

16:84318421:84322649

rs11645140

84322546

5.17E−07

4

NECAB2, MBTPS1, HSDL1, DNAAF1, KCNG4, WFDC1, ATP2C2

22

17:51482920:52487345

rs146709267

52065109

1.48E−06

11

MBTD1, UTP18, CA10, AC102948.2, C17orf112, KIF2B, TOM1L1, COX11, STXBP4, HLF, MMD, ANKFN1, NOG

  1. aPositions are based on Human Genome version 19 (hg19), build 37.
  2. bNumber of SNPs in the genomic locus (r2 ≥ 0.6 with any of the independent significant SNPs).