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SNP Report
| Name | rs2268026 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr3:52744331 - 52744331(1) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | T | ||
| Minor Allele | C | ||
| Minor Allele Frequence | 0.332468 | ||
| Functional Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000487068); intron_variant(ENST00000233027, ENST00000383721, ENST00000461689, ENST00000493199, ENST00000535191); non_coding_transcript_variant(ENST00000493199) | ||
| No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
| Source | Literature | ||
| Overlap with SZ? | NO | ||
| Overlap with MDD? | YES | ||
| Reference | Statistical Result | Description | Result Category |
|---|---|---|---|
| Major Depressive Disorder Working Group of the Psychiatric, G. C., 2013 | P-value=0.007732, OR=1.063 for MDD, P-value=0.00000003412, OR=1.099 for combined sample | In the combined analysis of these 819 SNPs, 15 exceeded genome-wide significance and all were in a 248 kb interval of high LD on 3p21.11. | Positive |


