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SNP Report
| Name | rs3794808 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr17:30204775 - 30204775(1) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Minor Allele | C | ||
| Minor Allele Frequence | 0.482029 | ||
| Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000261707, ENST00000394821, ENST00000401766, ENST00000579221, ENST00000581633); NMD_transcript_variant(ENST00000579221); non_coding_transcript_variant(ENST00000581633); upstream_gene_variant(ENST00000578609) | ||
| No. of Studies | 2 (Positive: 0; Negative: 2; Trend: 0) | ||
| Source | Literature | ||
| Overlap with SZ? | NO | ||
| Overlap with MDD? | YES | ||
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 |
|---|---|---|---|
| Soronen, P.,2011 | For MDD, allele, P-value = 0.0046;For Mood, allele, P-value = 0.0115, OR=0.8167, P-value(perm)=0.432 | Significant association was found. | Positive |



