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SNP Report
| Name | rs1108580 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr9:133639992 - 133639992(1) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | G | ||
| Minor Allele | G | ||
| Minor Allele Frequence | 0.429912 | ||
| Functional Annotation | intron_variant; splice_region_variant; synonymous_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000263611); splice_region_variant(ENST00000393056); synonymous_variant(ENST00000393056) | ||
| No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
| Source | Literature | ||
| Overlap with SZ? | NO | ||
| Overlap with MDD? | NO | ||


