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SNP Report
| Name | rs1539628 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr10:22638943 - 22638943(1) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | G | ||
| Minor Allele | G | ||
| Minor Allele Frequence | 0.272764 | ||
| Functional Annotation | downstream_gene_variant; intron_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000605011); intron_variant(ENST00000376573, ENST00000545335) | ||
| 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 |
|---|---|---|---|
| Jamra, R. A., 2006 (a) | ARMITAGE P-value = 0.544 for Schizophrenia | In the single marker analysis, none of the analyzed variants revealed significant association to disease status, neither for schizophrenia nor for BPAD. | Negative |



