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SNP Report
| Name | rs10462018 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr1:7819567 - 7819567(1) | ||
| Variant Alleles | C/G/T | ||
| Ancestral Allele | C | ||
| Minor Allele | T | ||
| Minor Allele Frequence | 0.109225 | ||
| Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000361923, ENST00000377532, ENST00000451646, ENST00000613533, ENST00000614998); non_coding_transcript_variant(ENST00000451646) | ||
| No. of Studies | 1 (Positive: 0; Negative: 1; 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 |
|---|---|---|---|
| Mansour, H. A., 2006 | TDT P-value = 0.197, Trends test=0.878 for Pittsburgh SZ/SZA | Negative |



