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SNP Report
| Name | rs3916965 dbSNP Ensembl |
|---|---|
| Location | chr13:105451011 - 105451011(1) |
| Variant Alleles | C/T |
| Ancestral Allele | C |
| Minor Allele | T |
| Minor Allele Frequence | 0.36222 |
| No. of Studies | 6 (Positive: 2; Negative: 4; Trend: 0) |
| Source | Literature |
| Overlap with SZ? | YES |
| Overlap with MDD? | NO |
| Reference | Statistical Result | Description | Result Category |
|---|---|---|---|
| Detera-Wadleigh, S. D., 2006 | Fisher P-value = 0.0001 for all, P-value = 0.0002 for SCZ Only | When results are combined across studies and phenotypes, this marker showed significant combined p value. Combined results in schizophrenia are significant for several markers and are highly significant (p<0.001) for three markers spanning more than 82 kb. | Positive |
| Bass, N. J.,2009 | chi-squared tests:for SCZ, allele, X2(1 d.f.)=2.101, P-value = 0.147 | No significant association was observed. | Negative |


