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SNP Report
| Name | rs449074 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chrCHR_HSCHR6_MHC_COX_CTG1:28571531 - 28571531(1) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | C | ||
| Minor Allele | C | ||
| Minor Allele Frequence | 0.0690895 | ||
| Functional Annotation | downstream_gene_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000452236, ENST00000530247, ENST00000508341) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||
SNPs in LD with rs449074 (count: 0) View in gBrowse (chrCHR_HSCHR6_MHC_COX_CTG1:28571531..28571531 )
