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SNP Report
| Name | rs2675968 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr2:232871534 - 232871534(1) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Minor Allele | T | ||
| Minor Allele Frequence | 0.287141 | ||
| Functional Annotation | downstream_gene_variant; intron_variant; upstream_gene_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000448993); intron_variant(ENST00000331342, ENST00000409230, ENST00000409533); upstream_gene_variant(ENST00000449331, ENST00000467665, ENST00000476690, ENST00000481155) | ||
| No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
| Source | Literature | ||
| Overlap with SZ? | YES | ||
| Overlap with MDD? | NO | ||
| Reference | Statistical Result | Description | Result Category |
|---|---|---|---|
| Andreassen OA, 2013 | Conditional FDR; SCZ loci given BD: P-value=0.0000564, FDR=0.143, FDR=0.021 for SCZ and BD | To estimate the number of independent loci, we 'pruned' the associated SNPs (removed SNPs with linkage disequilibrium (LD)>0.2), and identified a total of 58 independent loci with a significance threshold of conditional FDR<0.19. | Positive |


