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SNP Report
| Name | rs4663627 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr2:235887904 - 235887904(1) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Minor Allele | T | ||
| Minor Allele Frequence | 0.40615 | ||
| Functional Annotation | intron_variant; NMD_transcript_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000304032, ENST00000336665, ENST00000409538, ENST00000428334, ENST00000448025, ENST00000614409, ENST00000635100); NMD_transcript_variant(ENST00000635100) | ||
| 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=0.000131, FDR=0.203, FDR=0.033 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<0.20. | Positive |


