Table 2.
Chromosome | Base-pair position* | Nearest gene | Alleles | Frequency† | p value | Best-fit model (BIC)‡ | |
---|---|---|---|---|---|---|---|
Bipolar disorder 7 | |||||||
rs937l601 | 6 | 152832266 | SYNE1 | T/G | 0·346 | 4·27×10−9 | BPD |
rs10994397 | 10 | 61949130 | ANK3 | T/C | 0·065 | 7·08×10−9 | BPD |
rs4765914§,¶ | 12 | 2290157 | CACNA1C | T/C | 0·204 | 1·52×10−8 | BPD, MDD, schizophrenia |
rs12576775 | 11 | 78754841 | ODZ4 | G/A | 0·175 | 4·40×10−8 | BPD |
Schizophrenia 6 | |||||||
rs2021722 | 6 | 30282110 | MHC | C/T | 0·789 | 2·18×10−12 | Schizophrenia |
rs1625579 | 1 | 98275522 | MIR137 | T/G | 0·801 | 1·59×10−11 | ASD, schizophrenia |
rs12966547§ | 18 | 50903015 | CCDC68 | G/A | 0·588 | 2·60×10−10 | BPD, MDD, schizophrenia |
rs7914558§ | 10 | 104765898 | CNNM2 | G/A | 0·587 | 1·82×10−9 | MDD, schizophrenia |
rs11191580§ | 10 | 104896201 | NT5C2 | T/C | 0·911 | 1·11×10−8 | Five disorder |
rs7004633 | 8 | 89829427 | MMP16 | G/A | 0·184 | 2·75×10−8 | Schizophrenia |
rs10503253 | 8 | 4168252 | CSMD1 | A/C | 0·193 | 4·14×10−8 | Schizophrenia |
rs17662626§ | 2 | 193692866 | PCGEM1 | A/G | 0·915 | 4·65×10−8 | ASD, schizophrenia |
rs548181 | 11 | 124966919 | STT3A | G/A | 0·884 | 8·87×10−7 | Schizophrenia |
rs17512836 | 18 | 51345959 | TCF4 | C/T | 0·027 | 1·05×10−6 | ASD, schizophrenia |
Peak SNPs in associated region after clumping. BIC=Bayesian information criteria. BPD=bipolar disorder. MDD=major depressive disorder. ASD=autism spectrum disorders.
Detected with University of California Santa Cruz Genome Browser (version hg18).
Risk allele frequency in controls.
Best-fit multinomial logistic model by BIC (appendix pp 46-50 [bipolar disorder] and 51-61 [schizophrenia] provide a comparison of BIC and Akaike information criteria across models).
The BIC for the best and second best models do not differ significantly (ie, greater than 2 as previously suggested26).
rs4765914 is a proxy SNP for rs4765913 based on linkage disequilibrium (481 base pairs away, r2=0·874).