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SNP Report
| Name | rs2799573 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr10:18312999 - 18312999(1) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | T | ||
| Minor Allele | C | ||
| Minor Allele Frequence | 0.126398 | ||
| Functional Annotation | intron_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000282343, ENST00000324631, ENST00000352115, ENST00000377319, ENST00000377328, ENST00000377331, ENST00000396576, ENST00000615785, ENST00000617363) | ||
| No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
| Source | Literature | ||
| Overlap with SZ? | YES | ||
| Overlap with MDD? | YES | ||
| Reference | Statistical Result | Description | Result Category |
|---|---|---|---|
| Cross-Disorder Group of the Psychiatric Genomics Consortium,2013 | Association analysis:P-value = 0.0000000429,OR(95%CI) = 1.08(1.05-1.12) when five disorders were combined | Significant association was observed in cross-disorder analysis. | Positive |
| Reference | Statistical Result | Description | Result Category |
|---|---|---|---|
| Cross-Disorder Group of the Psychiatric Genomics Consortium,2013 | Association analysis:P-value = 0.0000000429,OR(95%CI) = 1.08(1.05-1.12) when five disorders were combined | Significant association was observed in cross-disorder analysis. | Positive |


