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. 2013 Oct 29;3:3075. doi: 10.1038/srep03075

Table 1. Genome wide significant variants following SCZ meta analysis.

Gene rsID CHR BP (hg18) Freq Pval Direction effect A1 A2 HetPVal Imputed
SDCCAG8 rs10927013 1 241655779 0.436 8.09 × 10−9 ++++++++++++++++ G T 0.91 Y
  rs2039839 1 241665293 0.564 1.28 × 10−8 −−−−−−−−−−−−−−−− A G 0.93 I
  rs6703335 1 241675590 0.562 3.71 × 10−9 −−−−−−−−−−−−−−−+ A G 0.91 I
ITIH1 rs2710323 3 52790945 0.466 2.97 × 10−8 −++−++−+++++++++ C T 0.39 A
MHC rs9379858 6 26475668 0.106 1.42 × 10−8 +++−++−++−++++++ C T 0.35 A
  rs3799380 6 26575161 0.220 2.80 × 10−8 +++−++−+++++++++ C T 0.82 I
  rs6456728 6 26585758 0.779 2.36 × 10−8 −−−+−−+−−−−−−−−− A G 0.82 I
  rs7749305 6 27554545 0.100 2.57 × 10−8 +++−++++++++++++ C T 0.29 Y
  rs6904596 6 27599278 0.896 3.06 × 10−8 −−−+−−−−−−−−−−−− A G 0.27 A
  rs17750424 6 27809101 0.085 1.99 × 10−8 ++++++++++++++++ C T 0.38 Y
  rs17693963 6 27818144 0.904 1.61 × 10−9 +++−++++++++++++ A C 0.36 I A5
  rs34706883 6 27913234 0.909 3.14 × 10−8 ++++++++++++++++ A C 0.39 Y
  rs13212651 6 27914964 0.909 3.34 × 10−8 ++++++++++++++++ A G 0.39 Y
  rs13194781 6 27923618 0.909 3.51 × 10−8 ++++++++++++++++ A G 0.42 A
  rs13199772 6 27942064 0.909 3.40 × 10−8 ++++++++++++++++ A G 0.42 Y
MAD1L1 rs10275045 7 1887352 0.403 2.16 × 10−8 −+−+−−−−−−−+−−−+ C T 0.36 N
  rs12537914 7 1914885 0.365 2.03 × 10−8 −+−+−−−−−−−+−−−− C T 0.47 Y
  rs4721184 7 1917310 0.369 2.74 × 10−8 +−+−+++++++−+++− C T 0.47 Y
  rs2056480 7 1920827 0.632 1.54 × 10−8 −−−+−−−−−−−+−−−+ A G 0.56 I
  rs4721190 7 1921258 0.596 3.83 × 10−8 −−−+−−−−−−−+−−−+ A G 0.69 I A5
  rs12699477 7 1935479 0.352 8.78 × 10−9 +−+++++++++−++++ C T 0.67 A
  rs2280550 7 1943082 0.639 3.80 × 10−8 −+−+−−−−−−−+−−−+ A G 0.49 Y
  rs12666575 7 1970947 0.358 8.27 × 10−10 −−−−−−+−−−−+−−−+ C T 0.19 A
  rs4721295 7 2003195 0.378 6.23 × 10−10 +−++++−++++−+++− G T 0.07 I
  rs1107592 7 2007958 0.62 5.64 × 10−9 +−++++−++++−+++− A G 0.04 I A5
  rs3778969 7 2106516 0.633 6.43 × 10−9 −−−−−−+−−−−+−−−+ A G 0.16 N
  rs10224497 7 2116493 0.574 1.09 × 10−8 ++++++−++++−+++− A G 0.13 I A5
  rs10239050 7 2124916 0.615 1.11 × 10−8 +−++++−++++−+++− A G 0.12 A
  rs3800913 7 2129763 0.604 4.03 × 10−8 ++++++−++++−+++− A G 0.15 A
  rs3800917 7 2134465 0.64 2.29 × 10−9 −+−−−−+−−−−+−−−+ A G 0.22 I
  rs3778991 7 2138981 0.656 2.21 × 10−9 −−−−−−+−−−−+−−−− A G 0.20 A
  rs3778994 7 2142381 0.616 2.53 × 10−9 −−−−−−+−−−−+−−−− A C 0.21 A5
  rs4721441 7 2150586 0.356 9.41 × 10−10 ++++++−++++−++++ C T 0.29 Y
  rs3779003 7 2151428 0.347 2.33 × 10−9 −−−−−−+−−−−+−−−− C T 0.23 I A5
  rs3757440 7 2239462 0.647 1.98 × 10−8 ++++++++++−−+++− A G 0.28 I A5
  rs7787274 7 2242519 0.651 1.08 × 10−8 −−−−−−−−−−−+−−−+ A G 0.21 Y
  rs7799006 7 2244752 0.350 1.24 × 10−8 −−−−−−−−−−−+−−−+ C T 0.23 A
CSMD1 rs6558872 8 4225547 0.571 4.75 × 10−8 −−−−+−−−−+−−−−−+ A G 0.46 I A5
TSNARE1 rs10098073 8 143307411 0.535 9.05 × 10−9 ++−+++++++++++++ A C 0.93 I
  rs4129585 8 143310840 0.566 2.38 × 10−8 ++++++++++++++++ A C 0.99 I

The final column lists the imputation status of each SNP. Y: imputed in all cohorts; N: not imputed; I: imputed in cohorts genotypes on the Illumina chips; A: imputed in cohorts genotyped on the Affymetrix chips; A5: imputed in cohorts genotyped on the Affymetrix 5.0 and 500 arrays.

HHS Vulnerability Disclosure