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SNP Report
| Name | rs954581 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr13:105499917 - 105499917(1) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | T | ||
| Minor Allele | C | ||
| Minor Allele Frequence | 0.119609 | ||
| Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000448407); non_coding_transcript_variant(ENST00000448407) | ||
| No. of Studies | 7 (Positive: 0; Negative: 7; Trend: 0) | ||
| Source | Literature | ||
| Overlap with SZ? | YES | ||
| Overlap with MDD? | NO | ||
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.
| Reference | Statistical Result | Description | Result Category |
|---|---|---|---|
| Detera-Wadleigh, S. D., 2006 | Fisher P-value = 0.5966 for all, P-value = 1 for SCZ Only | Negative | |
| Williams, N. M., 2006 | allelic P-value = 0.67 in Schizophrenia | We found no evidence for allelic or genotypic association with any of the polymorphisms studied for schizophrenia. We observed nominally significant evidence (P=.01-.047) for allelic association with 3 of the polymorphisms for bipolar disorder and significant evidence for whole-gene association (P=.04). | Negative |



