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SNP Report
| Name | rs6580038 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr5:153753281 - 153753281(1) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | T | ||
| Minor Allele | C | ||
| Minor Allele Frequence | 0.28115 | ||
| Functional Annotation | intron_variant; upstream_gene_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000285900, ENST00000340592, ENST00000448073, ENST00000518142, ENST00000518783, ENST00000521843); upstream_gene_variant(ENST00000476596) | ||
| No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
| Source | Literature | ||
| Overlap with SZ? | NO | ||
| 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.



