Search SNP
Search Gene
Search CNV
Search Haplotype
Search Other Variant
Search Region
Search Pathway
Search Study
SNP Report
| Name | rs1341402 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr13:105463160 - 105463160(1) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | T | ||
| Minor Allele | C | ||
| Minor Allele Frequence | 0.0742811 | ||
| Functional Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000610818, ENST00000613021); intron_variant(ENST00000448407); non_coding_transcript_variant(ENST00000448407); upstream_gene_variant(ENST00000329625, ENST00000375936, ENST00000471432, ENST00000473269, ENST00000488534, ENST00000489237, ENST00000559369, ENST00000595812, ENST00000600388, ENST00000601240, ENST00000618629) | ||
| No. of Studies | 10 (Positive: 3; 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 |
|---|---|---|---|
| Williams, N. M., 2006 | allelic P-value = 0.82 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 |
| Schumacher, J.,2004 | Association analysis:allele P-value = 0.352, OR=1.14, genotype P-value = 0.55, OR=1.48 | No significant association was observed in SZ. | Negative |
| Detera-Wadleigh, S. D., 2006 | Fisher P-value = 0.0505 for all, P-value = 0.9667 for SCZ Only | Negative |



